Medical Device Manufacturer · TW , Taipei

Medeon Biodesign, Inc. - FDA 510(k) Cleared Devices

7 submissions · 7 cleared · Since 2015

Total

Cleared

Denied

Medeon Biodesign, Inc. has 7 FDA 510(k) cleared medical devices. Based in Taipei, TW.

Historical record: 7 cleared submissions from 2015 to 2020. Primary specialty: General & Plastic Surgery.

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

510(k) submissions have been managed by Lin & Associate, LLC as regulatory consultant.

Medeon Biodesign, Inc. is one of 352 FDA 510(k) medical device manufacturers from Taiwan in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Medeon Biodesign, Inc.

7 devices

1-7 of 7

Data Source

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

Last updated: May 28, 2026