# Orthomod, LLC

- Location (FDA's records): Dayton, OH
- FDA decisions: 1 (2026–2026): 1 510(k) clearance
- Product codes: ODP (1)
- Predicates its devices cite: 4 (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
- X-Spine Systems, Inc.: 1 (https://510kreport.com/company/x-spine-systems)
- Innovasis, Inc.: 1 (https://510kreport.com/company/innovasis)
- Amedica Corp.: 1 (https://510kreport.com/company/amedica)
- Medtronic Sofamor Danek USA, Inc.: 1 (https://510kreport.com/company/medtronic-sofamor-danek-usa)

## Recent decisions
- K242303: MOD-C (Apr 1, 2026)

Source page: https://510kreport.com/company/orthomod