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Light, Examination, Medical, Battery Powered

FDA product code KYT · Class 1 · General Hospital

605
Registered devices
10
Adverse events
1
Recalls
6
510(k) clearances

Devices with this code

Recent recalls

DateFirmReason
2023-03-20DermLite LLCIncorrect labeling; Package labeling contains a different serial number then the serial number on the product labeling.

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Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.

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Sourced from public U.S. FDA data. Informational only — not medical or regulatory advice. Not affiliated with the FDA.