# G & H Wire Co.

- Location (FDA's records): Greenwood, IN
- FDA decisions: 2 (1996–2008): 2 510(k) clearances
- Product codes: DZB (1), OAT (1)
- Predicates its devices cite: 3 (0 its own); citations of its devices by later devices: 0 (0 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- Ortho Organizers, Inc.: 1 (https://510kreport.com/company/ortho-organizers)
- Dentaurum: 1 (https://510kreport.com/company/dentaurum)
- T.O.a.D.S., LLC: 1 (https://510kreport.com/company/toads)

## Recent decisions
- K081393: Orthodontic Temporary Anchorage Implant Screw (Aug 21, 2008)
- K961754: Safety Release Module (Jul 10, 1996)

Source page: https://510kreport.com/company/g-h-wire