FDA applicant

Ritter Implants GmbH & Co. KG

Biberach, DE3 decisions2014–20190 recalls

FDA records 3 decisions for Ritter Implants GmbH & Co. KG (Biberach, DE) from 2014 to 2019: 3 510(k) clearances. All are in product code DZE (Implant, Endosseous, Root-Form). No recall is linked to its devices.

FDA’s records also spell it “Ritter Implants GmbH CO KG”.

Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) refreshed weekly, last Nov 3, 2026

FIG. A — Illustration, dental panel, where it files most

How often FDA has decided Ritter Implants GmbH & Co. KG’s devices, and how often a recall has named them.

FDA decisions per year

1in 2019

2014high 1 (2014) · low 0 (2015)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2014.

FIG. 1 — Ritter Implants GmbH & Co. KG by year, 2014–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

Planning a device like Ritter Implants GmbH & Co. KG’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.

See the 510(k) Report

Other applicant names beginning “Ritter”

FDA records each applicant name separately; these may or may not be the same firm.

Ritter Co. 10 Ritter Concept GmbH 1

Ritter Implants GmbH & Co. KG

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Ritter”