FDA Device Intelligence
HomeDevice types › HQG

Lens, Spectacle, Non-Custom (Prescription)

FDA product code HQG · Class 1 · Ophthalmic

536
Registered devices
22
Adverse events
4
Recalls
56
510(k) clearances

Devices with this code

Recent recalls

DateFirmReason
2020-03-18Frames DirectThe firm has become aware through their optical laboratory supplier that prescription spectacle lenses within various frames failed to meet safety specificatio
2014-09-12Eyemart Express LtdPrescription eyeglass safety lenses did not meet specifications.
2014-02-26Wal Mart Stores, IncFifteen pairs of prescription, safety glasses did not meet required, industrial lens thickness; nor did these glasses have the OSHA-required manufacturer markin
2010-06-30Luxottica Optical ManufacturingThe polycarbonate prescription lenses may not meet the frame manufacturer's minimum lens thickness specification of 2.0 millimeters. LNAD made the decision to

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Sourced from public U.S. FDA data. Informational only — not medical or regulatory advice. Not affiliated with the FDA.