Medical Device Manufacturer · US , Irvine , CA

Bausch and Lomb, Inc., - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 2016

Total

Cleared

Denied

Bausch and Lomb, Inc., has 1 FDA 510(k) cleared medical devices. Based in Irvine, US.

Historical record: 1 cleared submissions from 2016 to 2016. Primary specialty: Ophthalmic.

Browse the FDA 510(k) cleared devices submitted by Bausch and Lomb, Inc., Filter by specialty or product code using the sidebar.

Bausch and Lomb, Inc., is one of 4777 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Bausch and Lomb, Inc.,

1 devices

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