Medical Device Manufacturer · US , La Jolla , CA

Fixano SA - FDA 510(k) Cleared Devices

5 submissions · 5 cleared · Since 2001

Total

Cleared

Denied

Fixano SA has 5 FDA 510(k) cleared medical devices. Based in La Jolla, US.

Historical record: 5 cleared submissions from 2001 to 2002. Primary specialty: Orthopedic.

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

Fixano SA is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Fixano SA

5 devices

1-5 of 5