# Ritter Implants GmbH & Co. KG

- Location (FDA's records): Biberach, DE
- FDA decisions: 3 (2014–2019): 3 510(k) clearances
- Names in FDA's records: Ritter Implants GmbH & Co. KG (2); Ritter Implants GmbH CO KG (1)
- Product codes: DZE (3)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 0 (0 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Recent decisions
- K180183: Ritter Dental Implant System (Jan 24, 2019)
- K160475: Ritter Dental Implant System (Dec 14, 2016)
- K131557: Ritter Implant System (May 9, 2014)

Source page: https://510kreport.com/company/ritter-implants