# Ceterix Orthopaedics, Inc.

- Location (FDA's records): Fremont, CA
- FDA decisions: 3 (2015–2018): 3 510(k) clearances
- Product codes: GAT (3)
- Predicates its devices cite: 4 (2 its own); citations of its devices by later devices: 2 (2 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
- Cayenne Medical, Inc.: 1 (https://510kreport.com/company/cayenne-medical)
- Teleflex Medical: 1 (https://510kreport.com/company/teleflex-medical)

## Its most-cited devices
- K180531: NovoStitch Pro Meniscal Repair System (2018), cited by 1
- K143356: NovoStitch Plus Meniscal Repair System (2015), cited by 1

## Recent decisions
- K181772: NovoStitch Pro Meniscal Repair System, CTX-A004 (size 0) (Aug 1, 2018)
- K180531: NovoStitch Pro Meniscal Repair System (Mar 29, 2018)
- K143356: NovoStitch Plus Meniscal Repair System (Jul 21, 2015)

Source page: https://510kreport.com/company/ceterix-orthopaedics