Data / Medical devices / Germany / Bego Bremer Goldschlaegerei Wilh. Herbst GMBH & Co. KG
Bego Bremer Goldschlaegerei Wilh. Herbst GMBH & Co. KG: FDA-registered device maker in Bremen, Germany, 3 510(k) clearances
Bego Bremer Goldschlaegerei Wilh. Herbst GMBH & Co. KG is registered with the FDA (registration 9611514) in Bremen, Germany. It lists 10 device types. The FDA files 3 510(k) clearances under its listings, the newest dated November 9, 2023. Registered through 2026. FDA data exported November 3, 2026.
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- FDA registration number
- 9611514
- FEI number
- 3002806467
- Address
- Wilhelm-Herbst-Strasse 1, Bremen, Germany, 28359
- Owner or operator
- BEGO BREMER GOLDSCHLAEGEREI WILH. HERBST GMBH & CO (8010221)
- Roles
- Manufacturer
- First device listed
- February 28, 1978
- Registered through
- 2026
- Brand names listed
- AuroLloyd M, BEGOCER G, BegoPal 300, BegoPal S, BegoStar, BegoStar ECO, Bio PontoStar XL, CoCr DG1 and more
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Additively Manufactured, Preformed, Resin Denture Tooth | PZY | 2 | Manufacturer | accessdata.fda.gov |
| Alloy, Gold-Based Noble Metal | EJT | 2 | Manufacturer | accessdata.fda.gov |
| Alloy, Metal, Base | EJH | 2 | Manufacturer | accessdata.fda.gov |
| Alloy, Other Noble Metal | EJS | 2 | Manufacturer | accessdata.fda.gov |
| Band, Elastic, Orthodontic | ECI | 1 | Manufacturer | accessdata.fda.gov |
| Band, Material, Orthodontic | DYO | 1 | Manufacturer | accessdata.fda.gov |
| Bracket, Metal, Orthodontic | EJF | 1 | Manufacturer | accessdata.fda.gov |
| Crown And Bridge, Temporary, Resin | EBG | 2 | Manufacturer | accessdata.fda.gov |
| Material, Tooth Shade, Resin | EBF | 2 | Manufacturer | accessdata.fda.gov |
| Retainer, Screw Expansion, Orthodontic | DYJ | 1 | Manufacturer | accessdata.fda.gov |
510(k) clearances
The 510(k) numbers this establishment lists, with the FDA decision on each. The applicant is the company that holds the clearance.
| Decided | 510(k) number | Device | Product code | Decision | Applicant | Source |
|---|---|---|---|---|---|---|
| November 9, 2023 | K233596 | VarseoSmile TriniQ | EBF | Substantially Equivalent | Bego Bremer Goldschlägerei Wilh. Herbst GmbH & Co. KG | accessdata.fda.gov |
| June 23, 2020 | K201668 | VarseoSmile Crown plus | EBF | Substantially Equivalent | Bego Bremer Goldschlägerei Wilh. Herbst GmbH & Co. KG | accessdata.fda.gov |
| May 18, 2020 | K193553 | VarseoSmile Temp | EBG | Substantially Equivalent | Bego Bremer Goldschlagerei Wilh. Herbst GmbH & Co. KG | accessdata.fda.gov |
Compare with other makers
- All makers of Alloy, Other Noble Metal
- All makers of Crown And Bridge, Temporary, Resin
- All makers of Material, Tooth Shade, Resin
- All makers of Alloy, Metal, Base
- All makers of Alloy, Gold-Based Noble Metal
- All makers of Band, Material, Orthodontic
Updated November 9, 2023. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.