Neurology in Florida

C2C Development, LLC is an FDA-registered, ISO 13485:2016-certified contract manufacturer and product development firm specializing in medical device design, prototyping, and low-volume manufacturing. The company operates a certified ISO 7 (Class 10,000) cleanroom environment and serves medical device innovators across laparoscopic, endoscopic, orthopedic, intravascular, neurological, stereotactic, and drug delivery applications. Services include comprehensive design control and prototyping using 3D modeling, 3D printing, conventional machining, and CNC machining; component sourcing and supplier qualification under ISO 13485 quality systems; assembly and packaging operations including kitting, cleaning, and inspection; verification and validation testing including packaging seal integrity, shelf-life, and mechanical/functional testing; sterilization management and laboratory testing coordination; and regulatory strategy consultation and submission support. The firm specializes in manual and semi-automated assembly for products that larger OEMs may not accommodate, enabling manufacturers to scale from pilot production to commercial release under either C2C's or the client's quality system. Clients include Medtronic, FHC, Monteris, and other established medical device manufacturers.

MEGIN Oy is a global leader in magnetoencephalography (MEG) technology for functional neuroimaging. The company develops and markets MEG Maps™, an integrated end-to-end solution powered by TRIUX™ neo hardware and MEG review™ software, designed for presurgical evaluation, clinical neurology, neurosurgery, and neuroscience research. MEG technology detects small magnetic fields generated by active brain cells, enabling real-time, non-invasive localization of brain activity to within centimeters or millimeters. MEGIN's systems are non-invasive, silent, radiation-free, and unaffected by skull properties or hemodynamic confounds, offering advantages over traditional fMRI and other functional imaging modalities. The TRIUX™ neo represents an advanced acquisition system with improved signal-to-noise ratios and advanced signal analysis capabilities. MEG Maps™ integrates scan acquisition, database management, and analysis functionality for clinical workflows. The company's solutions are deployed in hospitals and research institutions worldwide, including Mayo Clinic, Amsterdam UMC, Boys Town National Research Hospital, and major research centers. Applications include presurgical mapping for epilepsy and tumor surgery, epilepsy diagnosis and monitoring, brain tumor assessment, traumatic brain injury evaluation, stroke research, neurodegenerative disease investigation (Parkinson's, dementia), PTSD research, and pharmaceutical Phase I/III drug development. MEGIN serves neurology, neurosurgery, oncology, psychiatry, and neuroscience research markets globally.

Somatics, LLC manufactures the Thymatron® System IV, an FDA-cleared Class II medical device for electroconvulsive therapy (ECT). The Thymatron is indicated for treatment of catatonia or severe major depressive episodes associated with major depressive or bipolar disorder in patients age 13 and older who are treatment-resistant or require rapid treatment response. The device incorporates proprietary computer methods for optimal stimulus delivery, seizure quality analysis, and seizure endpoint determination, with multiple redundant error-protection levels. Treatment data is automatically compiled in end-of-treatment reports. Somatics provides GPD (proprietary Windows-based software) free to all Thymatron users, enabling real-time trace monitoring, patient database management, treatment storage and review, and HL7-compliant electronic data interfacing to major EHR systems including Epic, Cerner, Rhapsody, Mirth, and Corepoint. The company has over 80 years of history in ECT device development, with the first ECT patient treated in 1938.

Digitimer North America, LLC is the exclusive importer and distributor of Digitimer Ltd. (UK) products for the USA, Canada, and Mexico. Digitimer Ltd. has over 50 years of experience designing and manufacturing electronic instrumentation for medical researchers, practitioners, laboratories, hospitals, and universities. The company specializes in precision measurement and stimulation devices for research and clinical applications. Product lines include human physiology and research instrumentation, animal and cellular tissue research equipment, pediatric surgery devices, and brain tissue preservation systems (brain slice chambers and keepers). Their portfolio comprises extracellular amplifiers, mains noise eliminators, and specialized electrophysiology equipment. Digitimer is recognized for producing reliable, high-quality electronic instrumentation with an established reputation in academic medical centers, including endorsement from Harvard Medical School. The company serves the research community across neuroscience, physiology, pediatric surgery, and cellular biology disciplines. Products are designed to meet the precision requirements of laboratory and clinical settings, with emphasis on signal integrity and measurement accuracy.

evonos is a German medical device manufacturer based in Tuttlingen that specializes in neurosurgical instruments, implants, and operating room lighting systems. The company develops and manufactures high-quality surgical products designed in close collaboration with neurosurgeons to address specific clinical and ergonomic needs in the operating room. Product portfolio includes the evoDrill single-use cranial perforator, evoFix skull fixation and osteosynthesis systems, evoShape patient-specific skull implants (PEEK-based), evoFrame single-use retraction systems, evoLight operating room illumination systems, evoBase titanium head holder/fixation system, evoClip Raney scalp clips and applicators, evoBite laminectomy punches and rongeurs, and evoCarat diamond knives for neurosurgical applications. The company emphasizes product innovation driven by surgeon feedback, focusing on ergonomics (reduced force requirements), precise fit, and reduced patient irritation. Products are manufactured in Germany to ISO and regulatory standards. evonos serves leading surgeons and surgical centers globally with a focus on neurosurgical specialties. The company actively participates in international medical trade shows and maintains an educational blog covering neurosurgical topics and clinical conditions.

Digitimer Ltd. is a manufacturer of electrophysiology equipment and medical scientific instruments with over 50 years of operational history. The company designs and manufactures biological amplifiers for extracellular, intracellular, EEG, and EMG electrophysiological recording; electrical stimulators for in vitro, animal, and human applications including evoked potential testing, nerve excitability assessment, and intraoperative monitoring; pulse generators; and signal conditioning devices. The product portfolio includes the modular NeuroLog System, a compact versatile electrophysiology workstation suitable for amplification, pulse generation, signal conditioning, and stimulation across diverse research applications. Digitimer's human neurophysiology range features CE-marked and FDA-cleared electrical stimulators and amplifiers for clinical neurophysiology, neurodiagnostics, intraoperative monitoring, cognitive neuroscience, sports physiology, and behavioral psychology research. The company manufactures the DS7AP muscle locating stimulator, which is CE Medical Device Directive certified and FDA cleared for pediatric surgical applications in anorectal reconstruction (Peña/PSARP techniques). Digitimer also supplies urodynamic and manometry products including proprietary disposable catheters, urethral and rectal catheters, pessaries, and continence aids. The company represents multiple partner manufacturers including Alpha MED Scientific, Automate Scientific, Narishige, and Scientific Systems Design, expanding the breadth of electrophysiology and life science research equipment available through its distribution network.

Neuro20 Technologies Corp. manufactures FDA-cleared wearable neuromuscular electrical stimulation (EMS) systems designed for rehabilitation, physical therapy, and movement recovery. Their core product is the Neuro20 Smart Suit, a full-body wearable system paired with the Neuro20 PRO software and Control Box. The platform delivers customized electrical stimulation to individual muscle groups, enabling simultaneous multi-channel stimulation that the company claims cannot be replicated by conventional EMS devices. Applications include neurological conditions (multiple sclerosis, stroke, long COVID, spinal cord injury, Parkinson's, ALS, Guillain-Barré), orthopedic rehabilitation, chronic pain management, post-surgical recovery, and sports/fitness performance. The system is designed for both clinical use and home therapy. Key therapeutic benefits claimed include increased muscle strength and range of motion, improved blood circulation and synovial fluid, enhanced lymphatic drainage, reduced muscle spasms and atrophy, pain relief, and muscle re-education for dormant or paralyzed muscle groups. The device is non-invasive, drug-free, and portable. Neuro20 serves patients, medical providers (physical therapists, chiropractors, primary care), and research institutions. The company markets globally and provides clinical support, training, and ongoing research collaboration.

MEGIN is a global leader in magnetoencephalography (MEG) technology for functional neuroimaging. The company develops integrated solutions for clinical neurology, neurosurgery, and research applications. MEGIN's flagship product is MEG Maps™, powered by TRIUX™ neo hardware and MEG review™ software, providing seamless acquisition, database management, and analysis capabilities for presurgical evaluation and brain mapping. MEG (magnetoencephalography) is a non-invasive, real-time functional brain imaging modality that detects the small magnetic fields generated by active brain cells. MEGIN's technology localizes brain function to within centimeters or millimeters, identifying normal and abnormal activity without applied magnetic fields, radiation, or injections. The system is unaffected by skull and scalp, complementing hemodynamic data from MRI and other modalities (fMRI, PET, SPECT, TMS). Key clinical applications include presurgical evaluation and surgical planning for epilepsy, brain tumors, and neurological disorders; intracranial EEG (iEEG) placement guidance; and research in epilepsy, traumatic brain injury, PTSD, stroke, dementias, and Parkinson's disease. MEG is used in Phase I and III pharmaceutical drug development for neural mechanism assessment. Installed systems serve leading hospitals and research institutions worldwide, including Mayo Clinic, Boston Children's Hospital, Amsterdam UMC, University of Cambridge, and Swinburne University. MEGIN maintains headquarters in Espoo, Finland, with production facilities in Helsinki, and regional offices in the UK and Japan.

Orthomerica Products, Inc. is a global technology innovator and leading manufacturer of prefabricated, semi-custom, and custom orthoses since 1989. Based in Orlando, Florida, with over 240 employees, the company specializes in orthotic device design and manufacturing for the orthopedic and orthotics & prosthetics industries. Orthomerica serves 32+ countries and has impacted over 128,000 patients through its comprehensive product portfolio. The company offers innovative solutions spanning adult and pediatric orthoses, prosthetics, and cranial remolding devices such as the STARband system and Newport Hip Orthosis family. Beyond manufacturing, Orthomerica provides ABC-certified clinical education courses on orthotic topics, including lower extremity and cranial remolding specialties, along with dedicated customer support services. Known for precision craftsmanship, quality commitment, and continuous innovation, Orthomerica combines advanced 3D scanning technology, proprietary software, and additive manufacturing to deliver customized solutions addressing patient needs from head to toe.

LifeSync is a vertically-integrated manufacturer and direct supplier of cardiac cables, leadwires, and neuromonitoring connections for patient monitoring and diagnostic applications. The company specializes in ECG/cardiac monitoring cables, EMG electrodes for muscle and nerve testing, EEG electrodes for brain monitoring, intraoperative neuromonitoring (IONM) tools, nerve conduction study (NCS) supplies, and polysomnography (PSG) accessories. LifeSync positions itself as a single-source alternative to expensive OEM connections from multiple suppliers, emphasizing cost-effectiveness without compromising signal quality and radiolucency. The company manufactures radiolucent leadwires designed to provide clear signal and unobstructed imaging views during diagnostic procedures. LifeSync also offers custom design, manufacturing, and fulfillment services for medical cables and connections through its contract manufacturing division. The company maintains vertical integration across product design, manufacturing, and customer service. Leadership includes executives with 20+ years of experience in medical device development and operations at companies including Johnson & Johnson, GE Healthcare, Philips Healthcare, and 3M Healthcare. LifeSync serves global healthcare providers, hospital systems, and medical device manufacturers. The company operates from Coral Springs, Florida, with same-day shipping available on orders placed by 2 PM EST.

SleepMed Incorporated

SleepMed Incorporated is the largest private provider of sleep diagnostics and ambulatory EEG services in the United States. Founded in December 1999, the company specializes in solutions for sleep disorders and related chronic conditions through a network of hospital-based, physician-based, and freestanding sites. SleepMed has established itself as a leader in healthcare IT, focusing on improving clinical outcomes for patients. The company offers a range of services, including in-lab sleep studies and cloud-based Home Sleep Testing (HST) for obstructive sleep apnea (OSA) diagnosis. Their ambulatory EEG services utilize DigiTrace technology, and they provide therapy devices for sleep patients. With nearly 100,000 sleep studies and over 25,000 days of ambulatory EEG testing performed annually, SleepMed is well-equipped to address the needs of hospitals, sleep centers, home care settings, and physicians.

MYOLYN is a medical technology company specializing in functional electrical stimulation (FES) therapy systems for neuro-rehabilitation. Founded in 2013 and based in Gainesville, Florida, the company designs and manufactures the MyoCycle FES Cycling Therapy System—an FDA-cleared device that enables individuals with paralysis, spinal cord injuries, multiple sclerosis, stroke, cerebral palsy, and traumatic brain injury to engage in therapeutic cycling exercise. The MyoCycle uses electrical impulses to stimulate weak or paralyzed leg muscles, facilitating active movement and functional outcomes in both home and clinical settings. Available in two variants—MyoCycle Home for personal use and MyoCycle Pro for healthcare facilities—the system features automated calibration, personalized therapy protocols, and simplified controls. MYOLYN emphasizes comprehensive customer support, including clinical guidance from licensed therapists, insurance reimbursement assistance, and a 60-day satisfaction guarantee. The company partners with the U.S. Department of Veterans Affairs and rehabilitation centers nationwide.

Integer Holdings Corporation (NYSE: ITGR) is a global leader in medical device contract development and manufacturing (CDMO), with 80+ years of expertise in advanced medical device design, outsourcing, and component manufacturing. The company specializes in cardiac rhythm management, neuromodulation, vascular access, and cardiovascular devices. Integer operates through subsidiary brands Greatbatch Medical and Lake Region Medical, serving major global OEM medical device manufacturers across multiple therapeutic markets. The company designs and manufactures finished device systems and Class III medical devices, including catheters, guidewires, introducers, delivery systems, tantalum capacitors, implantable and external batteries, pacemaker batteries, implantable ports, and neuromodulation devices. Integer operates a vertically integrated supply chain with global R&D and manufacturing capabilities across four continents, supporting rapid prototyping, product development, testing and regulatory certification, product lifecycle management, and on-time delivery. The company serves 15+ medical device markets including cardiac rhythm management, neuromodulation, vascular access, cardiovascular, structural heart, electrophysiology, peripheral vascular, neurovascular, oncology, urology, infusion therapy, and hemodialysis. Integer is a manufacturing excellence organization with deep expertise in regulatory compliance, quality standards, and design optimization to minimize risk and accelerate time-to-market for OEM partners.

Carrier Medical, LLC is a leading distributor of medical equipment and solutions serving VA and DOD hospitals nationwide. The company specializes in providing high-quality medical devices across multiple specialties including neurology, sleep diagnostics, physical medicine and rehabilitation, respiratory care, and CPAP comfort products. Product lines include CPAP mask liners and headgear comfort covers made from bamboo organic fabric (Cloud brand); mobility and assistive devices such as rollators, knee walkers, transport chairs, and canes (PerfectFit, Phantom, Nova brands); and sleep diagnostic consumables including EEG electrodes and complete sensor kits (Dymedix brand). The company operates an e-commerce platform offering direct purchasing with nationwide fast shipping. Carrier Medical serves both institutional and individual customers, with documented experience supplying hospital inventory for multi-year partnerships. Products emphasize comfort, durability, and quality construction with features such as machine-washable liners and heavy-duty weight capacities. The company maintains customer support infrastructure and satisfaction guarantees.

Neurovirtual USA, Inc. is a global manufacturer of neurology and sleep medicine diagnostic equipment. The company specializes in advanced diagnostic systems for sleep medicine, neurology, and related clinical applications. Their product portfolio includes sleep study systems, EEG/EMG equipment, and ambulatory EEG monitoring solutions. Neurovirtual positions itself as a fast-growing provider committed to offering advanced diagnostic equipment at competitive pricing without compromising quality. The company serves healthcare facilities requiring neurology and sleep medicine diagnostic capabilities, with demonstrated presence at major medical conferences including SBNC (Sleep and Brain Disorders Conference) and epilepsy educational events. Manufacturing and distribution operate on a global scale. While specific regulatory certifications are not explicitly detailed in available marketing materials, the company's participation in professional medical conferences and focus on clinical diagnostics suggests compliance with relevant medical device standards.

BioSculptor Corporation designs, manufactures, and sells innovative solutions for orthopedic, podiatric, and prosthetics & orthotics (P&O) practices. The company specializes in cranial remolding orthoses and advanced scanning and milling technologies for custom device fabrication. Their primary product portfolio includes kinderBAND™, a custom-made cranial remolding helmet prescribed for plagiocephaly (infant head shape deformities), which holds FDA 510(k) clearance. The company also manufactures the BioScanner™, a rapid 3D scanning system capable of capturing patient anatomy in approximately 10 seconds, and the BioMill 4.5XF, a precision milling device designed to cut intricate shapes while preserving fine details for orthotic and prosthetic applications. These technologies enable P&O practitioners and orthopedic clinics to streamline workflow, improve fitting accuracy, and enhance patient outcomes. BioSculptor serves orthopedic surgeons, podiatrists, prosthetists, and orthotists across the United States. The company maintains manufacturing and support operations in Hialeah, Florida, and holds relevant regulatory clearances including FDA 510(k) for their cranial remolding devices.

SOMNOmedics GmbH is a German medical technology manufacturer specializing in portable, wearable diagnostic systems for sleep medicine, cardiology, and neurology. Founded approximately 20 years ago, the company develops and manufactures a comprehensive portfolio of sleep diagnostic equipment including polysomnography (PSG) systems, portable polygraphic devices, actigraphy monitors, and home sleep apnea testing solutions. Product lines include the SOMNO HD and SOMNO HD eco for in-lab and ambulatory polysomnography; SOMNOtouch RESP and SOMNOtouch RESP eco for respiratory polygraphic recordings; SOMNOwatch eco and SOMNOwatch plus for actigraphy and research applications; and specialized devices such as the O-Two Fellow for pulse oximetry and the NARCOguide for anesthesia depth monitoring. In cardiology, SOMNOmedics offers the SOMNOtouch NIBP for non-invasive continuous blood pressure measurement via pulse transit time (PTT) and the ABPMpro for oscillometric ambulatory blood pressure monitoring. The company also provides long-term EEG systems and insomnia diagnostics software. All devices are designed as modular, wearable systems with wireless connectivity options. SOMNOmedics emphasizes high-quality German manufacturing, invests 20% of revenue in R&D, and holds multiple patents in continuous blood pressure monitoring and wireless sensor technology. Products carry CE marking (referenced as 0297) indicating compliance with European Medical Device Regulation. The company provides 24/7 complimentary customer support and regular free software updates.

MCI Medical Concept Innovation manufactures advanced craniomaxillofacial and neurosurgical fixation systems specializing in osteosynthesis solutions. The company produces biocompatible surgical hardware including custom surgical plates, self-drilling screws, and cranial bone fixation devices engineered for trauma and reconstructive procedures. MCI utilizes premium ASTM F-67 titanium and other biocompatible materials with state-of-the-art manufacturing to meet rigorous medical device standards. The product portfolio addresses guided bone regeneration, maxillofacial reconstruction, and neuro-surgical applications requiring precision osteosynthesis.

EEG Software LLC develops and delivers neurofeedback software and training for clinical and at-home use. The company's flagship product, EEGer4, is a comprehensive neurofeedback suite that enables real-time EEG monitoring, live training feedback, and data review. EEGer4 supports remote and telehealth training modalities, integrates third-party amplifiers and therapeutic games, and is used across private practices, universities, regional healthcare networks, government agencies, and home-based clients in over 20 countries and all US states. The system is non-invasive and designed to help clinicians and clients with neurofeedback-based treatment for various conditions. EEG Software LLC offers BCIA-approved introductory training courses for clinicians and healthcare professionals, delivered by experienced practitioners and supported by clinical mentors throughout implementation and practice development. The company provides premium technical support for equipment setup, troubleshooting, and ongoing clinical operations. Founded and operated as a family business in Gainesville, Florida, the organization emphasizes practitioner-focused software design, flexibility in service delivery, and community support. The EEGer user community spans thousands of clinicians and includes universities and healthcare systems. The company maintains a privacy-first policy and offers comprehensive training curricula and continuing education opportunities.

Vycor Medical, Inc. operates two distinct business units specializing in neurosurgical and neurotherapeutic solutions. The primary division designs and manufactures neurosurgical medical devices, with the ViewSite Brain Access System (VBAS) as the flagship product—a minimally invasive neurosurgical device that improves access to brain lesions while reducing tissue damage. Clinical evidence from over 50 studies demonstrates VBAS results in reduced brain tissue trauma, minimized invasiveness, improved surgical visibility, and shortened operating and recovery times. The company's secondary business unit, NovaVision, develops non-invasive, computer-based vision rehabilitation therapies for patients with vision loss resulting from neurological trauma such as stroke. NovaVision Visual Restoration Therapy (VRT) is the only FDA-cleared therapy for vision rehabilitation following neurological brain damage; it is complemented by the NeuroEyeCoach program, which trains patients to make improved eye movements to enhance visual field detection. Vycor Medical serves neurosurgeons, neurologists, rehabilitation specialists, and vision care providers across hospital and outpatient settings. The company holds FDA regulatory clearance for its therapeutic products and demonstrates commitment to clinical validation and evidence-based outcomes.

UpRight Science develops FDA-cleared balance assessment and fall-risk detection technology for clinical and research use. The company's core offering is a medical-grade, AI-driven platform that quantifies balance and gait dynamics to identify fall risks, neurological decline, and medication side effects. Their technology integrates machine learning algorithms trained on biomechanical datasets to provide clinicians and researchers with actionable insights for patient stratification and early intervention. The platform is validated in clinical trials and marketed as addressing balance as "the sixth vital sign"—positioning fall prevention as a critical health metric alongside traditional vital signs. UpRight Science targets healthcare providers, physical therapy clinics, geriatric care facilities, and research institutions. The technology combines motion analysis with predictive analytics to detect deviations linked to neurodegenerative diseases and other conditions affecting balance and gait. The company emphasizes evidence-based development leveraging decades of balance science research. Their go-to-market approach includes direct sales to clinical and research institutions via demonstrations and proof-of-concept studies.

UR24Technology, Inc. manufactures the TrueClr™ External Catheter System, an FDA Class I medical device designed for non-invasive urinary management in adult and pediatric patients. TrueClr is a non-adhesive, portable external catheter system engineered to actively empty the bladder while preventing catheter-associated urinary tract infections (CAUTIs) commonly associated with indwelling catheters. The device is latex-free, hypoallergenic, and features a leak-proof design that prevents urine contact with skin, eliminating irritation and inflammation. All TrueClr systems are Medicare and Medicaid reimbursable. The product addresses a significant clinical need: CAUTIs account for approximately 80% of healthcare-associated UTIs and contribute to over 13,000 deaths annually. The company positions TrueClr as superior in function, comfort, and accessibility compared to competitive catheter systems. The device is suitable for multiple care settings including hospitals, long-term care facilities, and home care environments.

Applied Neuroscience develops advanced EEG (electroencephalography) analysis and neurofeedback software platforms for clinicians, researchers, and academic institutions. The company's flagship product, NeuroGuide™, is a comprehensive conventional and quantitative EEG (qEEG) system offering dynamic EEG databases, source localization analysis (swLORETA), coherence mapping, phase analysis, and 3D brain imaging capabilities. NeuroGuide enables real-time EEG visualization with dynamic color maps and automated clinical report generation. The platform supports Z-score neurofeedback protocols with surface, LORETA, and brain-computer interface training modes, including symptom-checklist-driven protocol preparation. NeuroNavigator™ adds current density Z-score mapping for precise functional brain network localization. Additional offerings include automatic clinical report writing integrated with Microsoft Office, expert clinical consultation services, and comprehensive training programs delivered through webinars and workshops. The company serves psychiatrists, neurologists, psychologists, neuropsychologists, and researchers across major universities including Drexel, Stanford, UC San Diego, and Swansea University. Products support conventional and quantitative EEG analysis with advanced metrics including phase locking, phase resetting, cross-frequency analysis, batch processing, and electrophysiological assessment tools.

MiniStim Corp manufactures the MiniStim PNS (Peripheral Nerve Stimulation) System, a minimally invasive, wireless implantable pulse generator (pIPG) designed for chronic pain management. The device is approximately 10 times smaller than existing battery-based neurostimulation systems and features a 4X power output (up to 24 mA) compared to competing PNS devices. Implantation occurs percutaneously under local anesthesia via a 3mm incision, with no requirement for general anesthesia or prolonged recovery. The wireless transmitter operates intuitively, allowing patients to control stimulation settings with a simple interface comparable to a television remote. Clinical applications include chronic neuropathic pain in the knee, hip, SI joint, and diabetic peripheral neuropathy. MiniStim conducts multiple prospective clinical trials (FLEX, TWIST, and TOUCH studies) to expand evidence and treatment indications. The implant is designed with a longevity of 10+ years. Remote patient support capabilities are integrated. The company emphasizes minimally invasive intervention and non-pharmaceutical pain management, positioning the system for patients seeking alternatives to opioids or those inadequately managed by conventional therapies. Manufacturing and clinical trial infrastructure support physician and facility enrollment.

Curonix LLC is a medical device manufacturer specializing in peripheral nerve stimulation (PNS) and spinal cord stimulation (SCS) systems for chronic pain management. The company's flagship product, the Freedom™ System, is a two-component permanent implant comprising an electrode array, implanted receiver, external transmitter assembly, and wearable accessory designed for minimally invasive treatment of chronic, intractable pain of peripheral nerve origin. The Freedom™ PNS System features NervPulse™ nerve-specific programming technology and wireless power delivery through clothing. Clinical evidence from a multicenter retrospective study in Germany demonstrated 62.5% pain reduction and 75% opioid medication reduction at 3–6 month follow-up in knee pain patients. The system is indicated for chronic pain management across multiple anatomical regions including knee, foot and ankle, shoulder, low back, and spine. Curonix serves both healthcare providers and patients globally, with regulatory presence in US and international markets. The company emphasizes MRI safety considerations for implanted systems and provides comprehensive professional education and patient resources. Manufacturing and device design are conducted to support minimally invasive surgical implantation protocols.

Black Forest Medical GmbH is a specialized neurosurgical equipment manufacturer headquartered in Germany with over 30 years of expertise in cranial stabilization and brain retraction systems. The company designs and manufactures the DORO® product line, a range of skull clamps and cranial fixation systems for neurosurgical procedures. The DORO LUCENT® Skull Clamp is optimized for intraoperative imaging environments, including CT, X-ray angiography, and fluoroscopy, featuring a patented one-handed release mechanism and interchangeable pin holders to accommodate patients from newborns to adults. DORO® systems are modular and compatible across multiple surgical table types, including standard OR tables, carbon-fiber surfaces, and spinal frames. Manufacturing is conducted at the company's German headquarters and selected partners in Switzerland and the USA. Black Forest Medical emphasizes quality management, evidence-based surgical workflows, and global technical support. The company has recently expanded applications to intraoperative MRI environments through partnerships with IMRIS. Products are designed for user-centric workflow integration with emphasis on surgical precision, patient safety, and navigation accuracy.

NeuroReformer® is an FDA-cleared Class II neuro-modulation device featuring patented micro-precision technology that delivers tailored, AI-calibrated neuro-frequencies for neural recovery and rehabilitation. Unlike conventional neuro-modulation devices using broad, unstable frequencies, NeuroReformer® replicates exact neurofrequency patterns that dynamically adapt during physical therapy movements. The system addresses axonal repair and cellular miscommunication resulting from injuries by restoring neural and neuromuscular signaling pathways, optimizing tissue repair, and accelerating nervous system function. Designed for clinical integration into physical therapy protocols, NeuroReformer® targets 100+ treatable anatomical regions and demonstrates 97%+ patient improvement rates. The device is indicated for chronic pain management, injury recovery, and rapid rehabilitation across diverse musculoskeletal and neurological conditions. Available for clinical use as of November 2025.