FDA Device Intelligence
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Lens, Multifocal Intraocular

FDA product code MFK · Class 3 · Ophthalmic

5,047
Registered devices
12,970
Adverse events
4
Recalls
0
510(k) clearances

Devices with this code

Recent recalls

DateFirmReason
2025-03-27Bausch & Lomb Surgical, Inc.In response to an increased number of reports of toxic anterior segment syndrome (TASS) in conjunction with implantation of enVista Aspire and enVista Envy IOLs
2006-12-14Alcon Laboratories, IncIntraocular lenses exposed to extreme temperatures while in storage.
2006-12-14Alcon Laboratories, IncIntraocular lenses exposed to extreme temperatures while in storage.
2006-12-14Alcon Laboratories, IncIntraocular lenses exposed to extreme temperatures while in storage.

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