FDA Device Intelligence
HomeDevice types › MJP

Lens, Intraocular, Toric Optics

FDA product code MJP · Class 3 · Ophthalmic

3,381
Registered devices
7,458
Adverse events
4
Recalls
0
510(k) clearances

Devices with this code

Recent recalls

DateFirmReason
2023-12-12Johnson & Johnson Surgical Vision, Inc.Due to intraocular lens containing an angle out of specification (OOS). The cylinder axis marks do not meet product specifications for the allowable angle betw
2021-08-06Johnson & Johnson Surgical Vision IncNonconforming product was distributed in error. Product was nonconforming due endotoxin levels higher than both the Firm's internal endotoxin specification lim
2021-01-27Johnson & Johnson Surgical Vision IncDue to the release of nonconforming Intraocular Lenses (IOLs).
2020-11-07Bausch & Lomb Surgical, Inc.Product may be missing toric axis marks.

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