Medical Device Manufacturer · US , Seattle , WA

Proprio, Inc. - FDA 510(k) Cleared Devices

4 submissions · 4 cleared · Since 2023

Total

Cleared

Denied

Proprio, Inc. has 4 FDA 510(k) cleared medical devices. Based in Seattle, US.

Latest FDA clearance: Dec 2025. Active since 2023. Primary specialty: Orthopedic.

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

FDA 510(k) cleared devices by Proprio, Inc.

4 devices

1-4 of 4