FDA Device Intelligence
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Drape, Patient, Ophthalmic

FDA product code HMT · Class 2 · General, Plastic Surgery

226
Registered devices
19
Adverse events
1
Recalls
7
510(k) clearances

Devices with this code

Recent recalls

DateFirmReason
2014-06-03Alcon Research, Ltd.The peel pouches of the Tray Support Covers may be insufficiently sealed so that sterility cannot be assured.

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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.