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
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| American Diagnostic Corp. | Hauppauge, NY, United States | Manufacturer, Repackager or relabeler | 0 | 0 | 0 | 0 | api.fda.gov | |
| Aspen Surgical Products, Inc. | Caledonia, MI, United States | Complaint file establishment, Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Belletorus Corporation | Cambridge, MA, United States | Repackager or relabeler, Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Bionix, LLC | Maumee, OH, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Beaver-Visitec International, Inc. | Waltham, MA, United States | Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Canfield Scientific, Inc. | Parsippany, NJ, United States | Complaint file establishment, Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Ceek Women's Health | Portland, OR, United States | Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Den-Mat Holdings, LLC | Lompoc, CA, United States | Complaint file establishment, Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Dentlight Inc. | Plano, TX, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| DermLite LLC | Aliso Viejo, CA, United States | Manufacturer | 0 | 0 | 1 | 0 | api.fda.gov | |
| Easy-Rn, LLC | Coral Springs, FL, United States | Remanufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Eusa Global LLC | Medley, FL, United States | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Firefly Global | Belmont, MA, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Firefly Vein Light LLC | Chattanooga, TN, United States | Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Forward Science Technologies LLC | Houston, TX, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| General Scientific Corp. | Ann Arbor, MI, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Hi-Tech Electronics | Oglesby, IL, United States | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Impact Innovations LLC | Boca Raton, FL, United States | Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Long Island Technology Group LLC | Woodbury, NY, United States | Contract manufacturer, Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Lumadent Inc | Reno, NV, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Linvatec Corporation | Largo, FL, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Medical Illumination International, Inc | Chatsworth, CA, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| North American Rescue, LLC. | Greer, SC, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Onlycare Inc | Denver, CO, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Quality Aspirators, Inc. | Dallas, TX, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Quality Aspirators, Inc. | Duncanville, TX, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Skinlens LLC | St Petersburg, FL, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Translite | Sugar Land, TX, United States | Manufacturer, Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Ultralight Optics Inc. | Westminster, CA, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Utah Medical Products, Inc. | Midvale, UT, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Xemax Surgical Products, Inc. | Napa, CA, United States | Specification developer | 0 | 0 | 0 | 0 | api.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.