Medical Device Manufacturer · US , Coral Gables , FL

Capillus, LLC - FDA 510(k) Cleared Devices

7 submissions · 7 cleared · Since 2015

Total

Cleared

Denied

Capillus, LLC has 7 FDA 510(k) cleared medical devices. Based in Coral Gables, US.

Historical record: 7 cleared submissions from 2015 to 2017. Primary specialty: General & Plastic Surgery.

Browse the FDA 510(k) cleared devices submitted by Capillus, LLC Filter by specialty or product code using the sidebar.

Capillus, LLC is one of 4735 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Capillus, LLC

7 devices

1-7 of 7