Laser & Energy Devices in Florida

360 Aesthetic Devices, LLC manufactures and distributes handheld microchanneling and skin rejuvenation devices for med spa professionals and beauty practitioners. The company's primary product line is the NanoStamp 360, an advanced skin rejuvenation device featuring interchangeable microchaneling and nano infusion treatment tips designed to address aging-related skin concerns including fine lines, wrinkles, acne scars, saggy skin, and stretch marks. The device is formulated with medical-grade serums and proprietary applicators for professional use in aesthetic treatment settings. NanoStamp 360 operates on a professional-only business model, requiring practitioners to register and sign in to access product catalogs, pricing, and training materials. The company provides comprehensive support to practitioners including treatment protocol development, financing options, certification and training programs via their Thinkific learning management system, marketing assistance, consent forms, and post-care guidance. Product offerings include the core NanoStamp 360 device (available in Grey and Teal color options), interchangeable treatment tips, compatible serums and supplies, and accessories. The company emphasizes treatment stacking and multi-session protocols designed to optimize collagen stimulation and client retention, and actively positions integration with complementary modalities such as exosomes, LED therapy, and other aesthetic treatments. 360 Aesthetic Devices operates from Naples, Florida and has sold thousands of devices globally. The company maintains an active social media presence and offers webinar-based education on advanced treatment applications and practitioner business development.

Endospheres manufactures professional aesthetic treatment devices for facial and body skin rejuvenation. The company produces non-invasive microvibration technology platforms designed for premium aesthetic clinics, spas, and beauty centers. Their primary product line, the Endospheres Evolution series, uses patented spherical roller technology to stimulate circulation, improve skin texture, refine tone, and address cellulite appearance through mechanical microvibration rather than laser or radiofrequency energy. Devices are marketed for comprehensive body and facial applications, with clinical validation cited from university and research institute studies. The Evolution All represents their flagship third-generation system, engineered for practitioners requiring reliable, reproducible aesthetic outcomes. All handpieces feature removable, sanitizable roller components to ensure hygiene and safety between treatments. The company emphasizes Italian engineering and design, positioning products in the premium professional segment. Endospheres operates in over 50 countries with a network of certified institutes and is recognized by major beauty publications including Elle, Grazia, and Marie Claire. Recent industry recognition includes Holy Grail Beauty Award 2025 (pro treatment category), Bella Beauty Awards (Coolest Tools), WellSpa 360 Readers' Choice 2024 (Best Body Device), and multiple international aesthetic technology awards. Products are marketed as non-surgical, non-invasive alternatives with no reported contraindications, designed for aesthetic clinics seeking repeatable treatment protocols and measurable patient outcomes.

DermaSensor Inc manufactures the DermaSensor device, an FDA-cleared, handheld optical spectroscopy system for non-invasive skin cancer detection at the point of care. The device uses elastic scattering spectroscopy (ESS) combined with proprietary artificial intelligence algorithms to analyze suspicious skin lesions and deliver malignancy risk assessment in approximately 30 seconds. Clinical data indicates 96% accuracy in detecting the three most common skin cancers: melanoma, basal cell carcinoma, and squamous cell carcinoma. The technology is designed for primary care physicians, family medicine practitioners, internal medicine doctors, plastic surgeons, and health systems seeking to improve skin cancer screening and reduce diagnostic uncertainty before dermatology referral. The device comprises a handheld probe that records five spectral recordings from the lesion; an integrated computer analyzes light scattering patterns to provide an "Investigate Further" or "Monitor" risk output. DermaSensor has completed 15 development, validation, and clinical utility studies encompassing over 5,000 diagnosed lesions. The company offers a 90-day introductory trial program, reimbursement guidance through partnership with The Reimbursement Group (TRG), e-learning training courses, cloud storage, remote device monitoring, and on-demand customer support. FDA 510(k) clearance and Breakthrough Device designation underscore regulatory validation. Markets served include family medicine practices, concierge services, internal medicine, health systems, and walk-in clinics across the United States.

Acuderm, Inc. is a 42-year-old US-based manufacturer and supplier of dermatological and surgical instruments, consumables, and devices headquartered in Fort Lauderdale, Florida. The company specializes in disposable and reusable surgical instruments for dermatology, plastic surgery, and general surgical applications. Core product lines include disposable biopsy punches (1–12 mm), disposable dermal curettes (1–7 mm), fine-gauge Acu-Needles with plastic hubs, and a comprehensive range of surgical instruments featuring tungsten carbide and non-tungsten carbide needle holders, forceps, scissors, and specialty instruments (Adson, Gradle, Webster, Metzenbaum, Spencer Stitch, Castroviejo, Olsen-Hegar, Halsey, Derf). The company also manufactures scalpel handles and blades, syringes, and dermatoscopes. A significant product category is surgical smoke evacuators, noted as award-winning systems for electrosurgical and laser applications. Additional offerings include cryosurgery equipment and electrosurgery devices. Acuderm manufactures many products in the USA and maintains a focus on quality, evidenced by supplier quality agreements. The company serves dermatologists, plastic surgeons, surgical centers, and hospitals. Distribution is supported by an e-commerce platform and direct sales channels.

Refine USA is a FDA-cleared manufacturer and supplier of medical aesthetic devices and science-backed skin solutions. The company designs, develops, and distributes innovative aesthetic treatment technologies for providers in the USA and internationally. Their product portfolio includes microneedling systems, platelet-rich plasma (PRP) devices, and advanced skincare solutions. All products are manufactured in the USA and undergo rigorous safety and efficacy validation. Refine USA serves aesthetic practitioners, dermatologists, and medical spas seeking evidence-based, clinically proven treatment options for skin rejuvenation, anti-aging, and advanced exfoliation procedures.

Sterex Electrolysis Intl., Ltd. is a UK-based manufacturer and distributor of electrolysis and diathermy equipment for professional aesthetic practitioners. The company specializes in electrical medical devices for hair removal and blemish removal across multiple settings including salons, clinics, dental practices, and podiatry services. Product applications include treatment of unwanted hair, age spots, moles, skin tags, warts, verrucae, sebaceous cysts, seborrhoeic keratosis, dermatosa papulosa nigra, xanthelasma, and vascular lesions (red veins, small blood spots, large blood spots/Campbell de Morgan spots). Sterex serves electrologists, beauty therapists, nurses in medical aesthetics, dentists, and podiatrists. The company operates a training division offering comprehensive courses on advanced electrolysis and cosmetic procedures, including specialized programs for transgender clients and PCOS-related hair removal. Sterex maintains a significant market presence in professional beauty and medical aesthetics through industry exhibitions and practitioner partnerships. The company markets itself as the trusted brand among electrologists globally. All product applications appear based on electrical modalities (electrolysis, diathermy) rather than laser or RF technologies. UK company registration number 01666827; VAT GB 378140052.

COSMOFRANCE is a medical aesthetics company specializing in minimally invasive aesthetic treatment devices and consumables. The company manufactures and distributes professional-grade equipment for dermatologists, plastic surgeons, and aesthetic practitioners. Primary product lines include the DermaSculpt microcannula system (available in multiple gauges from 22G–30G in various lengths), CosmoPen microneedling device with cartridge tips and collagen masks, and the ezPRF system (ezGEL platform) for platelet-rich fibrin and bio-stimulation therapies. Recent product launches include the CYTOGEN biocellulose restorative mask infused with bovine milk secretome and growth factors, and specialized microcannula sizes optimized for medium-viscosity injectables. The company is led by Medical Director Kian Karimi MD, FACS. Products are marketed toward aesthetic medicine practitioners for facial rejuvenation, post-treatment healing, and inflammatory response management. The company operates an e-commerce platform offering bulk purchasing discounts (5–20% off for 5–15+ boxes) and maintains an intranet-based resource system. No specific FDA 510(k), ISO 13485, or CE mark credentials are visible on the fetched homepage; regulatory status could not be confirmed from available content.

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