Medical Device Manufacturer · US , Salt Lake City , UT

OrthoGrid Systems, Inc. - FDA 510(k) Cleared Devices

4 submissions · 4 cleared · Since 2019

Total

Cleared

Denied

OrthoGrid Systems, Inc. has 4 FDA 510(k) cleared medical devices. Based in Salt Lake City, US.

Latest FDA clearance: May 2026. Active since 2019. Primary specialty: Radiology.

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

OrthoGrid Systems, Inc. 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 - OrthoGrid Systems, Inc.

4 devices

1-4 of 4