Medical Device Manufacturer · US , Woodstock , GA

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

7 submissions · 7 cleared · Since 1994

Total

Cleared

Denied

Spinalight, Inc. has 7 FDA 510(k) cleared medical devices. Based in Woodstock, US.

Historical record: 7 cleared submissions from 1994 to 2018. Primary specialty: Physical Medicine.

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

FDA 510(k) Regulatory Record - Spinalight, Inc.

7 devices

1-7 of 7