# Verticor, Ltd.

- Location (FDA's records): Round Rock, TX
- FDA decisions: 3 (2009–2011): 3 510(k) clearances
- Product codes: KWQ (1), MQP (1), HTY (1)
- Predicates its devices cite: 10 (0 its own); citations of its devices by later devices: 3 (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
- Synthes (Usa): 3 (https://510kreport.com/company/synthes-usa)
- Ortho Tec, LLC: 2 (https://510kreport.com/company/ortho-tec)
- X-Spine Systems, Inc.: 1 (https://510kreport.com/company/x-spine-systems)
- Synthes Spine: 1 (https://510kreport.com/company/synthes-spine)
- Alphatec Spine, Inc.: 1 (https://510kreport.com/company/alphatec-spine)
- Teleflex Medical Group: 1 (https://510kreport.com/company/teleflex-medical-group)
- Smt Schilling Metalltechnik GmbH: 1 (https://510kreport.com/company/smt-schilling-metalltechnik)

## Firms that cite its devices most
- Choicespine, LP: 1 (https://510kreport.com/company/choicespine)
- Amendia, Inc.: 1 (https://510kreport.com/company/amendia)
- Genesys Spine: 1 (https://510kreport.com/company/genesys-spine)

## Its most-cited devices
- K091426: Cervicore Corpectomy Cage (2009), cited by 2
- K103137: Venus Anterior Cervical Plate (2011), cited by 1

## Recent decisions
- K110047: Verticor K-Wire System (Feb 28, 2011)
- K103137: Venus Anterior Cervical Plate (Feb 10, 2011)
- K091426: Cervicore Corpectomy Cage (Dec 23, 2009)

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