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Data / Medical devices / Light, Examination, Medical, Battery Powered / United States

FDA-registered makers of Light, Examination, Medical, Battery Powered in the United States: 31 establishments

31 establishments in the United States are registered with the FDA to make Light, Examination, Medical, Battery Powered (product code KYT). 0 have a 510(k) clearance or PMA approval on file and 1 has a recall event. FDA data exported November 2, 2026.

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Device
Light, Examination, Medical, Battery Powered
Product code
KYT
Country
United States

Makers of Light, Examination, Medical, Battery Powered in the United States

MakerLocationRole510(k) clearancesLatest clearancePMA approvalsRecall eventsClass ISource
American Diagnostic Corp.Hauppauge, NY, United StatesManufacturer, Repackager or relabeler0000api.fda.gov
Aspen Surgical Products, Inc.Caledonia, MI, United StatesComplaint file establishment, Specification developer0000api.fda.gov
Belletorus CorporationCambridge, MA, United StatesRepackager or relabeler, Specification developer0000api.fda.gov
Bionix, LLCMaumee, OH, United StatesManufacturer0000api.fda.gov
Beaver-Visitec International, Inc.Waltham, MA, United StatesSpecification developer0000api.fda.gov
Canfield Scientific, Inc.Parsippany, NJ, United StatesComplaint file establishment, Manufacturer0000api.fda.gov
Ceek Women's HealthPortland, OR, United StatesSpecification developer0000api.fda.gov
Den-Mat Holdings, LLCLompoc, CA, United StatesComplaint file establishment, Manufacturer0000api.fda.gov
Dentlight Inc.Plano, TX, United StatesManufacturer0000api.fda.gov
DermLite LLCAliso Viejo, CA, United StatesManufacturer0010api.fda.gov
Easy-Rn, LLCCoral Springs, FL, United StatesRemanufacturer0000api.fda.gov
Eusa Global LLCMedley, FL, United StatesContract manufacturer0000api.fda.gov
Firefly GlobalBelmont, MA, United StatesManufacturer0000api.fda.gov
Firefly Vein Light LLCChattanooga, TN, United StatesSpecification developer0000api.fda.gov
Forward Science Technologies LLCHouston, TX, United StatesManufacturer0000api.fda.gov
General Scientific Corp.Ann Arbor, MI, United StatesManufacturer0000api.fda.gov
Hi-Tech ElectronicsOglesby, IL, United StatesContract manufacturer0000api.fda.gov
Impact Innovations LLCBoca Raton, FL, United StatesSpecification developer0000api.fda.gov
Long Island Technology Group LLCWoodbury, NY, United StatesContract manufacturer, Manufacturer0000api.fda.gov
Lumadent IncReno, NV, United StatesManufacturer0000api.fda.gov
Linvatec CorporationLargo, FL, United StatesManufacturer0000api.fda.gov
Medical Illumination International, IncChatsworth, CA, United StatesManufacturer0000api.fda.gov
North American Rescue, LLC.Greer, SC, United StatesManufacturer0000api.fda.gov
Onlycare IncDenver, CO, United StatesManufacturer0000api.fda.gov
Quality Aspirators, Inc.Dallas, TX, United StatesManufacturer0000api.fda.gov
Quality Aspirators, Inc.Duncanville, TX, United StatesManufacturer0000api.fda.gov
Skinlens LLCSt Petersburg, FL, United StatesManufacturer0000api.fda.gov
TransliteSugar Land, TX, United StatesManufacturer, Specification developer0000api.fda.gov
Ultralight Optics Inc.Westminster, CA, United StatesManufacturer0000api.fda.gov
Utah Medical Products, Inc.Midvale, UT, United StatesManufacturer0000api.fda.gov
Xemax Surgical Products, Inc.Napa, CA, United StatesSpecification developer0000api.fda.gov

Updated November 2, 2026. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.