Medical Device Manufacturer · US , Grand Rapids , MI

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

4 submissions · 4 cleared · Since 2011

Total

Cleared

Denied

Inrad, Inc. has 4 FDA 510(k) cleared medical devices. Based in Grand Rapids, US.

Latest FDA clearance: Apr 2025. Active since 2011. Primary specialty: General & Plastic Surgery.

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

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

4 devices

1-4 of 4