Medical Device Manufacturer · US , Carmel , IN

G & H Wire Co. - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 1996

2

Total

2

Cleared

0

Denied

FDA 510(k) Regulatory Record - G & H Wire Co. Dental ✕

2 devices

1-2 of 2

Cleared Aug 21, 2008

ORTHODONTIC TEMPORARY ANCHORAGE IMPLANT SCREW

Cleared Jul 10, 1996

SAFETY RELEASE MODULE

Data Source

Sourced from the FDA 510(k) public files . 175,218 total devices indexed.

Last updated: Apr 28, 2026