Bausch and Lomb, Incorporated

Bausch and Lomb, Incorporated holds 3 FDA 510(k) medical device clearances, first cleared 2018, most recent 2026, with 1 FDA device recall on record.

FDA recalls by Bausch and Lomb, Incorporated

Z-0672-2013 — Bausch and Lomb 27G sterile cannula packed in the Bausch and Lomb Amvisc 1.2% Sodium Hyaluronate ( Model 59051, 59081, 59051L, 59081L) and Amvisc Plus 1.6% Sodium Hyaluronate (Model 60081, 60051, 60051L, 60081L) ophthalmic viscosurgical device. The 27G disposable cannula is attached to the syringe standard luer fitting to deliver the Amvis or Amvis Plus during use as a surgical aid in opthalmic anterior or posterior segment procedures.Class I·Terminated·2012-11-15

Recalls are matched by FDA's recalling-firm name — openFDA's enforcement dataset doesn't reference 510(k) numbers, so a recall here may cover devices beyond this company's 510(k) clearances.

Recent clearances by Bausch and Lomb, Incorporated

Data sourced from openFDA. This site is unofficial and independent of the FDA.

Top product codes for Bausch and Lomb, Incorporated

FDA recalls by Bausch and Lomb, Incorporated

Recent clearances by Bausch and Lomb, Incorporated