Medical Device Manufacturer · US , Stillwater , MN

Proxy Biomedical , Ltd. - FDA 510(k) Cleared Devices

6 submissions · 6 cleared · Since 2005

Total

Cleared

Denied

Proxy Biomedical , Ltd. has 6 FDA 510(k) cleared medical devices. Based in Stillwater, US.

Historical record: 6 cleared submissions from 2005 to 2018. Primary specialty: General & Plastic Surgery.

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

510(k) submissions have been managed by Paladin Medical, Inc. as regulatory consultant.

Proxy Biomedical , Ltd. 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 - Proxy Biomedical , Ltd.

6 devices

1-6 of 6

Data Source

Sourced from the FDA 510(k) public files . 175,450 total devices indexed.

Last updated: Jun 08, 2026