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Frame, Spectacle

FDA product code HQZ · Class 1 · Ophthalmic

47,645
Registered devices
35
Adverse events
1
Recalls
198
510(k) clearances

Devices with this code

Recent recalls

DateFirmReason
2003-05-02Magnivision, Inc.Possibility of eye injury from large temple tags on promotional sale product when customer tries them on in store.

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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.