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Device, Medical Examination, Ac Powered
FDA product code KZF · Class 1 · General Hospital
390
Registered devices
401
Adverse events
5
Recalls
37
510(k) clearances
Devices with this code
Sim.LED 350 3p — S.I.M.E.O.N. Medical GmbH & Co. KGTri Star — SunnexACEMSO15F — ACEM SPACelestial Star — SunnexMI Product Line — Medical Illumination International Inc.Verilux — BEAR DOWN CONSULTINGNA — STERIS CORPORATIONChromophare — Berchtold Holding GmbHNA — STERIS CORPORATIONVerilux — BEAR DOWN CONSULTINGVerilux — BEAR DOWN CONSULTINGAMSCO — STERIS CORPORATIONVISIANO 10-1 — Derungs Licht AGMidmark — MIDMARK CORPORATIONCelestial Star — SunnexMidmark — MIDMARK CORPORATIONStarTrol — HUOT INSTRUMENTS, LLCErgon Boom Series — SKYTRON LLCCIRCLED — ACEM SPAStarTrol — HUOT INSTRUMENTS, LLCACEMST1 — ACEM SPARitter — MIDMARK CORPORATIONLUCEA LED® — MAQUET SASVista LED — Avante
Recent recalls
| Date | Firm | Reason |
|---|---|---|
| 2025-10-13 | MRIMed Inc. | Due to battery component overheating while charging resulting in melting of internal components and causing smoke. |
| 2017-04-21 | Stryker Communications | The exam light may have a tolerance issue with the adapter assembly, which could potentially not allow the snap ring to be seated correctly. If this is the cas |
| 2016-11-18 | Ohmeda Medical | Certain power cords could overheat. The affected power cords were manufactured by Electric-Cord and are referred to as Taller Bridge power cords. The overheatin |
| 2013-07-25 | Stryker Communications | Potential incomplete final weld on the drop tube flange. |
| 2004-02-19 | Burton Medical Products Corp | Pivot joint on these ceiling mount lights may fail and lights may fall onto patients. |
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