Data / Medical devices / Device, Medical Examination, Ac Powered / United States
FDA-registered makers of Device, Medical Examination, Ac Powered in the United States: 15 establishments
15 establishments in the United States are registered with the FDA to make Device, Medical Examination, Ac Powered (product code KZF). 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
- Device, Medical Examination, Ac Powered
- Product code
- KZF
- Country
- United States
Makers of Device, Medical Examination, Ac Powered in the United States
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Aadco Medical, Inc. | Randolph, VT, United States | Manufacturer | 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 | |
| Bear Down Brands, LLC | Fullerton, CA, United States | Complaint file establishment, Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Burton Medical LLC | Addison, IL, United States | Manufacturer, Repackager or relabeler | 0 | 0 | 0 | 0 | api.fda.gov | |
| GlobalMed Holdings, LLC | Scottsdale, AZ, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Huot Instruments, LLC | Menomonee Falls, WI, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Klyo Medical Systems Inc | Doral, FL, United States | Manufacturer, Repackager or relabeler | 0 | 0 | 0 | 0 | api.fda.gov | |
| LG Medical Design, LLC | Salt Lake City, UT, United States | Complaint file establishment, Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Lifeport, LLC. | Woodland, WA, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Midmark Corporation | Versailles, OH, 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 | |
| Steris Corporation | Montgomery, AL, United States | Complaint file establishment, Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| STRYKER Communications, Inc. | Flower Mound, TX, United States | Complaint file establishment, Specification developer | 0 | 0 | 2 | 0 | api.fda.gov | |
| Waldmann Lighting | Wheeling, IL, United States | Repackager or relabeler, Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Welch Allyn, Inc. | Skaneateles Falls, NY, United States | Manufacturer, 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.