Home › Device types › LPM
Lenses, Soft Contact, Extended Wear
FDA product code LPM · Class 3 · Ophthalmic
0
Registered devices
3,063
Adverse events
26
Recalls
0
510(k) clearances
Recent recalls
| Date | Firm | Reason |
|---|---|---|
| 2025-06-16 | CooperVision, Inc. | Lens blisters may have an incomplete or leaking seal which may render them unsterile. |
| 2025-06-16 | CooperVision, Inc. | Lens blisters may have an incomplete or leaking seal which may render them unsterile. |
| 2024-08-29 | CooperVision, Inc. | Manufactured with a misaligned axis resulting in lenses with the incorrect power, may experience poor visual acuity |
| 2024-08-29 | CooperVision, Inc. | Manufactured with a misaligned axis resulting in lenses with the incorrect power, may experience poor visual acuity |
| 2023-01-26 | CooperVision, Inc. | Manufactured with misaligned axis resulting in lenses with the incorrect power, users may experience poor visual acuity |
| 2023-01-26 | CooperVision, Inc. | Manufactured with misaligned axis resulting in lenses with the incorrect power, users may experience poor visual acuity |
| 2020-01-13 | CooperVision Inc. | Incorrect power of lenses than the expected |
| 2020-01-13 | CooperVision Inc. | Incorrect power of lenses than the expected |
| 2018-08-14 | Lens.com | The product may be counterfeit and could have microbial issues. |
| 2018-08-01 | Allied Vision Group Inc | Potentially counterfeit products in/and counterfeit packaging were imported to the U.S. |
Query this across every FDA database — by API.
Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.
Get your free API keyRead the docsSourced from public U.S. FDA data. Informational only — not medical or regulatory advice. Not affiliated with the FDA.