FDA Device Intelligence
HomeDevice types › MVN

Lens, Contact, (Disposable)

FDA product code MVN · Class 2 · Ophthalmic

1,052
Registered devices
372
Adverse events
16
Recalls
26
510(k) clearances

Devices with this code

Recent recalls

DateFirmReason
2025-08-22CooperVision, Inc.One lot manufactured with an invalid sterilization cycle.
2025-08-22CooperVision, Inc.One lot manufactured with an invalid sterilization cycle.
2025-08-22CooperVision, Inc.One lot manufactured with an invalid sterilization cycle.
2025-02-27CooperVision, Inc.a limited number of lots were manufactured with an incorrect cylinder power.
2024-03-20Ontact IncContact lenses recalled due to potential bacterial contamination.
2018-02-21CooperVision Inc.The secondary packaging is labeled with an incorrect expiration date.
2018-02-21CooperVision Inc.The secondary packaging is labeled with an incorrect expiration date.
2018-02-21CooperVision Inc.The secondary packaging is labeled with an incorrect expiration date.
2018-02-21CooperVision Inc.The secondary packaging is labeled with an incorrect expiration date.
2017-12-18Johnson & Johnson Vision Care, Inc.Package integrity failure observed during routine shift package integrity testing at an external re-packager.

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