# Creodent Prosthetics, Ltd.

- Location (FDA's records): New York, NY
- FDA decisions: 9 (2013–2022): 9 510(k) clearances
- Product codes: NHA (8), NXC (1)
- 510(k) review time since 2016: median 220 days, against 188 for FDA's reviews in the same codes and years (2 of 7 faster)
- Predicates its devices cite: 13 (7 its own); citations of its devices by later devices: 7 (7 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
- Straumann USA: 1 (https://510kreport.com/company/straumann-usa)
- Pou YU Biotechnology Co., Ltd.: 1 (https://510kreport.com/company/pou-yu-biotechnology)
- Nobel Biocare AB: 1 (https://510kreport.com/company/nobel-biocare)
- Zimmer Dental, Inc.: 1 (https://510kreport.com/company/zimmer-dental)
- Sweden & Martina S.P.A.: 1 (https://510kreport.com/company/sweden-martina)
- The Argen Corporation: 1 (https://510kreport.com/company/argen)

## Its most-cited devices
- K150012: CreoDent Solidex Customized Abutment (2015), cited by 5
- K162734: CreoDent Solidex Customized Abutment (2017), cited by 1
- K113738: Creodent Solidex Custom Abutment (2013), cited by 1

## Recent decisions
- K220390: CreoDent Solidex Customized Abutment and Screw (Dec 2, 2022)
- K211427: CREOKORREKT Aligners (Oct 13, 2022)
- K202909: CreoDent Solidex Customized Abutment (Apr 2, 2021)
- K202095: CreoDent Solidex Customized Abutment and Screw (Dec 16, 2020)
- K170100: CreoDent Solidex Customized Abutment and Screw (Jul 18, 2017)
- K162734: CreoDent Solidex Customized Abutment (May 8, 2017)
- K160436: CreoDent Solidex Custom Abutment (Sep 29, 2016)
- K150012: CreoDent Solidex Customized Abutment (Jun 4, 2015)

Source page: https://510kreport.com/company/creodent-prosthetics