# K131557: Ritter Implant System

- Pathway: 510(k) (Traditional)
- Applicant: Ritter Implants GmbH CO KG
- Decided: May 9, 2014 after 345 days
- Product code: DZE (Implant, Endosseous, Root-Form)
- Device class: 2
- Regulation: 21 CFR 872.3640
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
No later device cites it as a predicate yet.
0 of 1 device in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA’s file for it is a 510(k) statement, which names no predicate.

## Indications for use
The Ritter Implants are intended for simple or multiple replacements of lost teeth and provide a way to attach the prosthetic pieces in totally or partially edentulous patients. Ritter Implants are intended for immediate loading when good primary stability is achieved and with appropriate occlusal loading.

Source page: https://510kreport.com/device/K131557
Methodology: https://510kreport.com/methodology