FDA Device Intelligence
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Clamp, Penile

FDA product code FHA · Class 1 · Gastroenterology, Urology

49
Registered devices
26
Adverse events
1
Recalls
11
510(k) clearances

Devices with this code

Recent recalls

DateFirmReason
2018-02-16Aesculap Implant Systems LLCThe plastic sleeves of the Penis Clamp and Mouth Gag may stick together during or after reprocessing rendering the instruments unusable.

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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.