Medical Device Manufacturer · US , Broomall , PA

Keeler Limited - FDA 510(k) Cleared Devices

5 submissions · 5 cleared · Since 2014

Total

Cleared

Denied

Keeler Limited has 5 FDA 510(k) cleared medical devices. Based in Broomall, US.

Historical record: 5 cleared submissions from 2014 to 2015. Primary specialty: Ophthalmic.

Browse the FDA 510(k) cleared devices submitted by Keeler Limited Filter by specialty or product code using the sidebar.

Keeler Limited is one of 4867 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Keeler Limited

5 devices

1-5 of 5