FDA applicant

Bego Implant Systems GmbH & Co. KG

Bremen, DE3 decisions2009–20210 recalls

FDA records 3 decisions for Bego Implant Systems GmbH & Co. KG (Bremen, DE) from 2009 to 2021: 3 510(k) clearances. Most are in product codes DZE (Implant, Endosseous, Root-Form) and KCT (Sterilization Wrap Containers, Trays…). Its devices cite 4 predicates, 1 of them its own earlier devices. No recall is linked to its devices.

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 Bego Implant Systems GmbH & Co. KG’s devices, and how often a recall has named them.

FDA decisions per year

2in 2021

2009high 2 (2021) · low 0 (2010)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2009.

FIG. 1 — Bego Implant Systems GmbH & Co. KG by year, 2009–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

Planning a device like Bego Implant Systems 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 “Bego”

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

Bego U.S.A. 7 Bego Bremer Goldschlaegerei Wilh. Herbst GmbH & CO 4 Bego Bremer Goldschlägerei Wilh. Herbst GmbH & Co. KG 3

Bego Implant Systems GmbH & Co. KG

Which product codes does it file in?

Whose devices does it build on?

Which of its devices are cited most?

What has FDA decided for it lately?

Other applicant names beginning “Bego”