FDA applicant
Bego Bremer Goldschlägerei Wilh. Herbst GmbH & Co. KG
FDA records 3 decisions for Bego Bremer Goldschlägerei Wilh. Herbst GmbH & Co. KG (Bremen, DE) from 2020 to 2023: 3 510(k) clearances. Most are in product codes EBF (Material, Tooth Shade, Resin) and EBG (Crown And Bridge, Temporary, Resin). Since 2016 its 510(k)s took a median of 4 days from receipt to decision, against 190 for FDA’s reviews in the same codes and years. Its devices cite 2 predicates, 0 of them its own earlier devices. No recall is linked to its devices.
FDA’s records also spell it “Bego Bremer Goldschlagerei Wilh. Herbst GmbH & Co. KG”.
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) refreshed weekly
How often FDA has decided Bego Bremer Goldschlägerei Wilh. Herbst GmbH & Co. KG’s devices, and how often a recall has named them.
FDA decisions per year
1in 2023
2026 so far, outlined.
Recalls per year
No recall linked to its devices since 2020.
Planning a device like Bego Bremer Goldschlägerei Wilh.…’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) ReportOther applicant names beginning “Bego”
FDA records each applicant name separately; these may or may not be the same firm.