Capillus is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Capillus - FDA 510(k) Cleared Devices
Recent clearances: Capillus 112, Capillus 244
1
Total
1
Cleared
0
Denied
Capillus has 1 FDA 510(k) cleared medical devices. Based in Miami, US.
Historical record: 1 cleared submissions from 2019 to 2019. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Capillus Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Capillus
1 devices