Medical Device Manufacturer · US , Redwood City , CA

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

2 submissions · 2 cleared · Since 2018

Total

Cleared

Denied

Intravu, Inc. has 2 FDA 510(k) cleared medical devices. Based in Redwood City, US.

Latest FDA clearance: Dec 2024. Active since 2018. Primary specialty: Orthopedic.

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

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

2 devices

1-2 of 2