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Trabeculotome

FDA product code HMZ · Class 1 · Ophthalmic

24
Registered devices
26
Adverse events
1
Recalls
0
510(k) clearances

Devices with this code

Recent recalls

DateFirmReason
2025-09-06Iantrek Inc.Potential for compromised integrity of the sterile packaging.

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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.