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Lens, Intraocular, Accommodative

FDA product code NAA · Class 3 · Ophthalmic

605

Registered devices

1,402

Adverse events

1

Recalls

0

510(k) clearances

Devices with this code

Crystalens® AO IOL — Bausch & Lomb Incorporated enVista MX60 IOL — Bausch & Lomb Incorporated Crystalens Accommodating IOL (50) — Bausch & Lomb Incorporated Crystalens Accommodating IOL (AT-52AO) — Bausch & Lomb Incorporated enVista MX60 IOL — Bausch & Lomb Incorporated Crystalens® AO IOL — Bausch & Lomb Incorporated enVista MX60 IOL — Bausch & Lomb Incorporated enVista MX60 IOL — Bausch & Lomb Incorporated enVista MX60 IOL — Bausch & Lomb Incorporated enVista MX60 IOL — Bausch & Lomb Incorporated Crystalens Accommodating IOL (AT-52AO) — Bausch & Lomb Incorporated enVista MX60 IOL — Bausch & Lomb Incorporated enVista MX60 IOL — Bausch & Lomb Incorporated enVista MX60 IOL — Bausch & Lomb Incorporated Crystalens Accommodating IOL (AT-52AO) — Bausch & Lomb Incorporated CARDINAL HEALTH — Cardinal Health 200, LLC enVista MX60 IOL — Bausch & Lomb Incorporated enVista MX60 IOL — Bausch & Lomb Incorporated Crystalens Accommodating IOL (50) — Bausch & Lomb Incorporated enVista MX60 IOL — Bausch & Lomb Incorporated enVista MX60 IOL — Bausch & Lomb Incorporated Crystalens® AO IOL — Bausch & Lomb Incorporated enVista MX60 IOL — Bausch & Lomb Incorporated CARDINAL HEALTH — Cardinal Health 200, LLC

Recent recalls

Date	Firm	Reason
2011-11-14	Bausch and Lomb, Incorporated	Bausch + Lomb voluntary initiated the recall due to a physician complaint of haze on the Crystalens AO which was visualized using an angled beam from a slit lam

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