Medical Device Manufacturer · US , Seattle , WA

Spirit Ridge Technologies - FDA 510(k) Cleared Devices

5 submissions · 5 cleared · Since 1995

Total

Cleared

Denied

Spirit Ridge Technologies has 5 FDA 510(k) cleared medical devices. Based in Seattle, US.

Historical record: 5 cleared submissions from 1995 to 1995. Primary specialty: General & Plastic Surgery.

Browse the FDA 510(k) cleared devices submitted by Spirit Ridge Technologies Filter by specialty or product code using the sidebar.

Spirit Ridge Technologies 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 - Spirit Ridge Technologies

5 devices

1-5 of 5