Medical Device Manufacturer · KR , South Korea

Millimax Corp. - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 1989

2

Total

2

Cleared

0

Denied

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

2 devices

1-2 of 2

Cleared Nov 21, 1989

LATEX SURGICAL GLOVES

General Hospital · 223d

Cleared Sep 21, 1989

PATIENT EXAMINATION GLOVES

General Hospital · 162d

Data Source

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

Last updated: Apr 28, 2026