# Frontier Devices, Inc.

- Location (FDA's records): Pelham, AL
- FDA decisions: 1 (2010–2010): 1 510(k) clearance
- Product codes: JEY (1)
- Predicates its devices cite: 4 (0 its own); citations of its devices by later devices: 1 (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
- Bioplate, Inc.: 2 (https://510kreport.com/company/bioplate)
- Tekka: 1 (https://510kreport.com/company/tekka)
- Synthes (Usa): 1 (https://510kreport.com/company/synthes-usa)

## Firms that cite its devices most
- Impladent, Ltd.: 1 (https://510kreport.com/company/impladent)

## Its most-cited devices
- K091812: Frontier Devices Craniomaxillofacial, Cranio Closure, Orthognathic, Mandible Reconstruction and Mesh Systems (2010), cited by 1

## Recent decisions
- K091812: Frontier Devices Craniomaxillofacial, Cranio Closure, Orthognathic, Mandible Reconstruction and Mesh Systems (May 7, 2010)

Source page: https://510kreport.com/company/frontier-devices