# Rhausler, Inc.

- Location (FDA's records): San Carlos, CA
- FDA decisions: 2 (2011–2015): 2 510(k) clearances
- Product codes: ODP (1), OVE (1)
- Predicates its devices cite: 3 (1 its own); citations of its devices by later devices: 4 (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
- Spinal Elements, Inc.: 1 (https://510kreport.com/company/spinal-elements)
- Seaspine, Inc.: 1 (https://510kreport.com/company/seaspine)

## Firms that cite its devices most
- Orthopaedic Implant Company: 1 (https://510kreport.com/company/orthopaedic-implant)
- Alliance Partners, LLC: 1 (https://510kreport.com/company/alliance-partners)
- Acuity Surgical Devices, LLC: 1 (https://510kreport.com/company/acuity-surgical-devices)

## Its most-cited devices
- K111272: Rhausler Plage Anterior Cervical Fusion System (2011), cited by 4

## Recent decisions
- K150455: RT2 Trabeculite Titanium Cervical Cage System (Nov 19, 2015)
- K111272: Rhausler Plage Anterior Cervical Fusion System (Nov 29, 2011)

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