Home › Alcon Laboratories, Inc. › AcrySof™ IQ Vivity™
AcrySof™ IQ Vivity™
Alcon Laboratories, Inc. · Model DAT515 · UDI-DI 00380652428811
POE
Prescription
0
510(k) clearances
5,706
Adverse events
1
Recalls
16
Facilities
Description
Sterile UV Absorbing Acrylic Foldable Aspheric Wavefront-Shaping Toric Posterior Chamber Intraocular Lenses
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2023-07-06 | Johnson & Johnson Surgical Vision, Inc. | Their is a potential that intraocular lenses (IOLs) were manufactured with unintended toric fiducial marks. |
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 docsData compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.
