Medical Device Manufacturer · US , Doylestown , PA

Neoforce Group, Inc. - FDA 510(k) Cleared Devices

7 submissions · 7 cleared · Since 2006

Total

Cleared

Denied

Neoforce Group, Inc. has 7 FDA 510(k) cleared medical devices. Based in Doylestown, US.

Historical record: 7 cleared submissions from 2006 to 2011. Primary specialty: Anesthesiology.

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

510(k) submissions have been managed by Tuv America, Inc. as regulatory consultant.

Neoforce Group, Inc. is one of 18325 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Neoforce Group, Inc.

7 devices

1-7 of 7