Medical Device Manufacturer · US , Macon , GA

Syncro Medical Innovations, Inc. - FDA 510(k) Cleared Devices

6 submissions · 3 cleared · Since 2002

Total

Cleared

Denied

Syncro Medical Innovations, Inc. has 3 FDA 510(k) cleared medical devices. Based in Macon, US.

Historical record: 3 cleared submissions from 2002 to 2020. Primary specialty: Gastroenterology & Urology.

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

510(k) submissions have been managed by Keystone Regulatory Services, LLC as regulatory consultant.

Syncro Medical Innovations, Inc. is one of 12946 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Syncro Medical Innovations, Inc.

6 devices

1-6 of 6

Data Source

Sourced from the FDA 510(k) public files . 175,972 total devices indexed.

Last updated: May 28, 2026