FDA applicant

Bego Bremer Goldschlaegerei Wilh. Herbst GmbH & CO

Bremen, DE4 decisions1998–20130 recalls

FDA records 4 decisions for Bego Bremer Goldschlaegerei Wilh. Herbst GmbH & CO (Bremen, DE) from 1998 to 2013: 4 510(k) clearances. Most are in product codes EIH (Powder, Porcelain) and EJH (Alloy, Metal, Base). Its devices cite 3 predicates, 0 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 Bremer Goldschlaegerei Wilh. Herbst GmbH & CO’s devices, and how often a recall has named them.

FDA decisions per year

2in 2013

2007high 2 (2013) · low 0 (2007)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Bego Bremer Goldschlaegerei Wilh. Herbst GmbH & CO by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

Planning a device like Bego Bremer Goldschlaegerei Wilh.…’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.

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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 Implant Systems GmbH & Co. KG 3 Bego Bremer Goldschlägerei Wilh. Herbst GmbH & Co. KG 3

Bego Bremer Goldschlaegerei Wilh. Herbst GmbH & CO

Which product codes does it file in?

Whose devices does it build on?

Who builds on its devices?

Which of its devices are cited most?

What has FDA decided for it lately?

Other applicant names beginning “Bego”