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Lens, Contact (Other Material) - Daily
FDA product code HQD · Class 2 · Ophthalmic
102
Registered devices
134
Adverse events
5
Recalls
118
510(k) clearances
Devices with this code
BostonSight PROSE — The Boston Foundation For Sight, Inc.Optimum Classic — CONTAMAC HOLDINGS LIMITEDFluoroperm 151 — Paragon Vision Sciences, Inc.Custom Stable — Valley Contax, Inc.Boston EO — Bausch & Lomb IncorporatedAcuity — ACUITY POLYMERS, INC.Paraperm O2 — Paragon Vision Sciences, Inc.Boston XO — Bausch & Lomb IncorporatedMeniconZ (tisilfocon A) Blue — MENICON CO.,LTD.OP-3 — LAGADO CORPORATION, THEEyeSpace Scleral — Tianjin Mastervision Technology Co., Ltd.Optimum HR 1.53 — CONTAMAC HOLDINGS LIMITEDAcuity — ACUITY POLYMERS, INC.Fluoroperm 92 — Paragon Vision Sciences, Inc.SA-18 — LAGADO CORPORATION, THEParaperm EW — Paragon Vision Sciences, Inc.FSA 38 — Paragon Vision Sciences, Inc.EyeSpace Bespoke — Tianjin Mastervision Technology Co., Ltd.Acuity — ACUITY POLYMERS, INC.BostonSight SCLERAL — The Boston Foundation For Sight, Inc.BostonSight PROSE — The Boston Foundation For Sight, Inc.OP-2 — LAGADO CORPORATION, THEFLOSI — LAGADO CORPORATION, THEBoston II — Bausch & Lomb Incorporated
Recent recalls
| Date | Firm | Reason |
|---|---|---|
| 2025-06-10 | Boston Foundation For Sight | Select orders of lenses were manufactured with errors impacting sagittal height, haptics, or both. |
| 2025-06-10 | Boston Foundation For Sight | Select orders of lenses were manufactured with errors impacting sagittal height, haptics, or both. |
| 2018-07-03 | Alden Optical | Vials labeled for the prescriptions contained incorrect lenses |
| 2018-07-03 | Alden Optical | Vials labeled for the prescriptions contained incorrect lenses |
| 2010-04-20 | Bausch & Lomb Inc | The amount of D&C #6 Dye added to the formulation exceeded specified amounts. |
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