Medical Device Manufacturer · US , Carmel , IN

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

2 submissions · 2 cleared · Since 1996

Recent clearances: ORTHODONTIC TEMPORARY ANCHORAGE IMPLANT SCREW, SAFETY RELEASE MODULE

View 2 510(k) Devices ↓

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 . 176,325 total devices indexed.

Last updated: Sep 13, 2026