# Ortho-Pro, LLC

- Location (FDA's records): Round Rock, TX
- FDA decisions: 4 (2003–2011): 4 510(k) clearances
- Product codes: HWC (2), KWH (1), HRS (1)
- Predicates its devices cite: 6 (0 its own); citations of its devices by later devices: 10 (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
- Osteomed LP: 2 (https://510kreport.com/company/osteomed)
- Kinetikos Medical, Inc.: 1 (https://510kreport.com/company/kinetikos-medical)
- Sgarlato Laboratories, Inc.: 1 (https://510kreport.com/company/sgarlato-laboratories)
- Dow Corning Corp. Healthcare Industries Materials: 1 (https://510kreport.com/company/dow-corning-healthcare-industries-materials)
- Vilex, LLC: 1 (https://510kreport.com/company/vilex)

## Firms that cite its devices most
- Wrightmedicaltechnologyinc: 3 (https://510kreport.com/company/wrightmedicaltechnologyinc)
- Fusion Orthopedics, LLC: 2 (https://510kreport.com/company/fusion-orthopedics)
- Vilex, LLC: 1 (https://510kreport.com/company/vilex)
- Gramercy Extremity Orthopeidics, LLC: 1 (https://510kreport.com/company/gramercy-extremity-orthopeidics)
- Internal Fixation Systems, Inc.: 1 (https://510kreport.com/company/internal-fixation-systems)
- Orthopro, LLC: 1 (https://510kreport.com/company/orthopro)
- Integra LifeSciences Corporation: 1 (https://510kreport.com/company/integra-lifesciences)

## Its most-cited devices
- K042310: Ortho-Pro Cannulated Bone Screws (2004), cited by 4
- K032682: STS Screw (2003), cited by 3
- K094037: TC Plating System (2010), cited by 3

## Recent decisions
- K102601: Orthoflex Rod (Jan 14, 2011)
- K094037: TC Plating System (Mar 10, 2010)
- K042310: Ortho-Pro Cannulated Bone Screws (Sep 16, 2004)
- K032682: STS Screw (Oct 22, 2003)

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