# Ingen Orthopedics, LLC

- Location (FDA's records): Cranbury, NJ
- FDA decisions: 3 (2012–2013): 3 510(k) clearances
- Product codes: KWS (1), HSD (1), PHX (1)
- Predicates its devices cite: 10 (1 its own); citations of its devices by later devices: 1 (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
- Genesis Medical, Inc.: 2 (https://510kreport.com/company/genesis-medical)
- Tornier, Inc.: 2 (https://510kreport.com/company/tornier)
- DePuy Orthopaedics, Inc.: 1 (https://510kreport.com/company/depuy-orthopaedics)
- Exactech, Inc.: 1 (https://510kreport.com/company/exactech)
- Biomet Manufacturing Corp: 1 (https://510kreport.com/company/biomet-manufacturing)
- Zimmer, Inc.: 1 (https://510kreport.com/company/zimmer)
- Encore Medical L.P.: 1 (https://510kreport.com/company/encore-medical)

## Its most-cited devices
- K120374: Seviin Reverse Shoulder (2012), cited by 1

## Recent decisions
- K131277: Seviin Fracture Shoulder (Aug 28, 2013)
- K130635: Seviin Surface Replacement Shoulder (Aug 26, 2013)
- K120374: Seviin Reverse Shoulder (Jul 9, 2012)

Source page: https://510kreport.com/company/ingen-orthopedics