# Ortho Tec, LLC

- Location (FDA's records): California, CA
- FDA decisions: 22 (1999–2004): 22 510(k) clearances
- Product codes: KWP (9), MNH (6), MNI (4), KWQ (2), MQV (1)
- Predicates its devices cite: 3 (1 its own); citations of its devices by later devices: 7 (1 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
- Orthotec, Inc.: 2 (https://510kreport.com/company/orthotec)

## Firms that cite its devices most
- Biomatlante: 2 (https://510kreport.com/company/biomatlante)
- Verticor, Ltd.: 2 (https://510kreport.com/company/verticor)
- Intra-Lock International: 1 (https://510kreport.com/company/intra-lock-international)
- Choicespine, LP: 1 (https://510kreport.com/company/choicespine)

## Its most-cited devices
- K040514: Eovia Calcium Phosphate Ceramic (2004), cited by 3
- K030500: Oria Zenith (2003), cited by 2
- K021679: Oria Spinal Clip System (2002), cited by 1
- K001535: Zenith Plate System, Anterior Spinal Instrumentation (2001), cited by 1

## Recent decisions
- K040514: Eovia Calcium Phosphate Ceramic (May 3, 2004)
- K040346: Modification to Oria Top Clip System (Mar 12, 2004)
- K030958: Oria Spinal System, Domino and Tube Connectors (Nov 20, 2003)
- K031471: Oria Spinal Clip System, Lateral Intermediate Connector, Model AL01 (Oct 10, 2003)
- K023884: Modification Oria Spinal System (Aug 20, 2003)
- K023378: Oria Claris (Jun 27, 2003)
- K031452: Oria Spinal Clip System, Sacral Connector, Models CA03 and AO03 (Jun 18, 2003)
- K030500: Oria Zenith (Mar 20, 2003)

Source page: https://510kreport.com/company/ortho-tec