# Orthomatrix, Inc.

- Location (FDA's records): Collierville, TN
- FDA decisions: 8 (1984–2001): 8 510(k) clearances
- Product codes: LYC (3), HSB (2), JDQ (1), HWC (1), DZE (1)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 2 (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 that cite its devices most
- Dio Department Dsi, Inc.: 1 (https://510kreport.com/company/dio-department-dsi)
- Bioform, Inc.: 1 (https://510kreport.com/company/bioform)

## Its most-cited devices
- K852765: HA-2000 Hydroxylapatite (1985), cited by 2

## Recent decisions
- K010738: Cannulated Plus Screw System (Aug 1, 2001)
- K001254: Orthomatrix, Inc. Cerclage System (Dec 13, 2000)
- K992850: Magellan Tibial Intramedullary Nail (Mar 10, 2000)
- K992856: Magellan Humeral Intramedullary Nail (Mar 10, 2000)
- K852766: HA-1000 & HA-500 Hydroxylapatite Tooth Root Substi (Oct 21, 1985)
- K852765: HA-2000 Hydroxylapatite (Sep 23, 1985)
- K851367: HA-1000 & HA-500 Hydroxylapatite-Modification (May 21, 1985)
- K842163: Ridgematrix 20/40 Mesh, Periomatrix (Aug 9, 1984)

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