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Marker, Sclera

FDA product code HMQ · Class 1 · Ophthalmic

108
Registered devices
1
Adverse events
1
Recalls
0
510(k) clearances

Devices with this code

Recent recalls

DateFirmReason
2025-12-16Vortex Surgical Inc.There may be voids located in the seal of Tyvek pouches associated with identified catalog numbers and lots. A compromised sterile barrier has potential of biob

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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.