# Dentatus USA, Ltd.

- Location (FDA's records): New York, NY
- FDA decisions: 4 (1996–2004): 4 510(k) clearances
- Product codes: EBI (1), ELS (1), DZH (1), DZE (1)
- Predicates its devices cite: 12 (0 its own); citations of its devices by later devices: 4 (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
- Impla-Med: 2 (https://510kreport.com/company/impla-med)
- Denar Corp.: 2 (https://510kreport.com/company/denar)
- Artech Corp.: 2 (https://510kreport.com/company/artech)
- C.B.S. Biotechnics, Inc.: 1 (https://510kreport.com/company/cbs-biotechnics)
- Sendax Mdic Management, Inc.: 1 (https://510kreport.com/company/sendax-mdic-management)
- Bofors Nobelpharma, Inc.: 1 (https://510kreport.com/company/bofors-nobelpharma)
- Sherwood Medical Industries: 1 (https://510kreport.com/company/sherwood-medical-industries)
- Core-Vent Corp.: 1 (https://510kreport.com/company/core-vent)

## Firms that cite its devices most
- Odontit S.A.: 2 (https://510kreport.com/company/odontit)
- Implant Innovations, Inc.: 1 (https://510kreport.com/company/implant-innovations)
- Intra-Lock International: 1 (https://510kreport.com/company/intra-lock-international)

## Its most-cited devices
- K980620: Dentatus Mti  Modular Transitional Implants and Prosthetic System (1998), cited by 3
- K961704: Mti-MP Transitional Implants and Modular Prosthetic System (1996), cited by 1

## Recent decisions
- K042931: Tuf Link Silicone Reliner (Dec 8, 2004)
- K031793: Dentatus Osciomat (Nov 13, 2003)
- K980620: Dentatus Mti  Modular Transitional Implants and Prosthetic System (May 15, 1998)
- K961704: Mti-MP Transitional Implants and Modular Prosthetic System (Jul 26, 1996)

Source page: https://510kreport.com/company/dentatus-usa