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Lens, Contact (Other Material) - Daily

FDA product code HQD · Class 2 · Ophthalmic

68
Registered devices
134
Adverse events
5
Recalls
118
510(k) clearances

Devices with this code

Fluoroperm 92 — Paragon Vision Sciences, Inc.Acuity — ACUITY POLYMERS, INC.Boston 7 — Bausch & Lomb IncorporatedFLUOREX®500UV — G. T. LABORATORIES, INC.FLUOREX®300 — G. T. LABORATORIES, INC.SA-18 — LAGADO CORPORATION, THEOptimum Extreme — CONTAMAC HOLDINGS LIMITEDOptimum Classic — CONTAMAC HOLDINGS LIMITEDFLUOREX®700 — G. T. LABORATORIES, INC.SGP 3 — LIFESTYLE CO INC, THEParaperm EW — Paragon Vision Sciences, Inc.Optimum Comfort — CONTAMAC HOLDINGS LIMITEDFluoroperm 60 — Paragon Vision Sciences, Inc.HEXA100 — CONTAMAC HOLDINGS LIMITEDEyeSpace Bespoke — Tianjin Mastervision Technology Co., Ltd.Custom Stable — Valley Contax, Inc.OP-2 — LAGADO CORPORATION, THEBoston XO2 — Bausch & Lomb IncorporatedFLUOREX®500 — G. T. LABORATORIES, INC.FLOSI — LAGADO CORPORATION, THEONSI-56 — LAGADO CORPORATION, THEMeniconZ (tisilfocon A) Blue — MENICON CO.,LTD.Synergeyes Casted Buttons — SYNERGEYES, INC.Acuity — ACUITY POLYMERS, INC.

Recent recalls

DateFirmReason
2025-06-10Boston Foundation For SightSelect orders of lenses were manufactured with errors impacting sagittal height, haptics, or both.
2025-06-10Boston Foundation For SightSelect orders of lenses were manufactured with errors impacting sagittal height, haptics, or both.
2018-07-03Alden OpticalVials labeled for the prescriptions contained incorrect lenses
2018-07-03Alden OpticalVials labeled for the prescriptions contained incorrect lenses
2010-04-20Bausch & Lomb IncThe amount of D&C #6 Dye added to the formulation exceeded specified amounts.

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