Medical Device Manufacturer · US , Alpharetta , GA

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

6 submissions · 6 cleared · Since 2011

Total

Cleared

Denied

Carticept Medical, Inc. has 6 FDA 510(k) cleared medical devices. Based in Alpharetta, US.

Historical record: 6 cleared submissions from 2011 to 2015. Primary specialty: General Hospital.

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

510(k) submissions have been managed by Regulatory and Clinical Research Institute as regulatory consultant.

Carticept Medical, Inc. is one of 18390 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

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

6 devices

1-6 of 6

Data Source

Sourced from the FDA 510(k) public files . 176,325 total devices indexed.

Last updated: Sep 16, 2026