Medical Device Manufacturer · US , Cleveland , OH

Makintech Corp. - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 1989

2

Total

2

Cleared

0

Denied

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

2 devices

1-2 of 2

Cleared Jul 14, 1989

LATEX EXAMINATION GLOVES

General Hospital · 88d

Cleared Feb 03, 1989

LATEX SURGICAL GLOVE (NON STERILE)

General Hospital · 168d

Data Source

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

Last updated: Apr 28, 2026