Medical Device Manufacturer · KR , Seoul, Korea

Unidus Corp. - FDA 510(k) Cleared Devices

7 submissions · 7 cleared · Since 1989

7

Total

7

Cleared

0

Denied

FDA 510(k) Regulatory Record - Unidus Corp. General Hospital ✕

1 devices

1-1 of 1

Cleared Apr 11, 1989

SKIN ANGEL BRAND (PATIENT EXAM GLOVES - LATEX)

General Hospital · 15d

Data Source

Sourced from the FDA 510(k) public files . 175,730 total devices indexed.

Last updated: Apr 27, 2026