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BEGO Bremer Goldschlägerei Wilh. Herbst GmbH & Co.KG

US

Last updated May 24, 2026

What BEGO Bremer Goldschlägerei Wilh. Herbst GmbH & Co.KG makes

The company manufactures custom-made dental crowns made from polymer materials, as well as dental casting alloys—both noble and non-noble—used for fabricating dental restorations. It also produces temporary dental crowns and bridges in resin, resin-based artificial teeth, and dental brazing alloys for joining components. Examples include polymer crown systems like VarseoSmile TriniQ and Crown plus, along with resin-based temporary restorations and resin artificial teeth.

These dental devices are classified as Class II under FDA regulations and are authorised through the 510(k) pathway or listed under the UDI system. The company’s products are registered with the FDA in the United States. No additional regulatory bodies or jurisdictions are referenced in the provided data.

Written from this company's registered devices by an AI model, and not verified by a human reviewer.

Frequently asked questions

What types of medical devices does BEGO Bremer Goldschlägerei Wilh. Herbst GmbH & Co.KG manufacture?

BEGO specialises in dental devices, primarily custom-made dental crowns made from polymer materials, dental casting alloys (both noble and non-noble), temporary resin crowns and bridges, resin artificial teeth, and dental brazing alloys. These products are designed for dental restorations and repairs, such as long-term crowns, temporary fixes, and alloy-based frameworks.

Where is BEGO Bremer Goldschlägerei Wilh. Herbst GmbH & Co.KG based, and which regulatory registries list its devices?

BEGO operates in the United States, where its dental devices are registered with the FDA. The company’s products are listed in the FDA’s 510(k) clearance registry and the Unique Device Identifier (UDI) system, ensuring traceability and compliance with U.S. regulatory requirements for Class II devices.

How are BEGO’s dental devices classified under FDA regulations?

BEGO’s dental devices fall under Class II classification by the FDA. This classification applies to devices that pose moderate risk and require special controls—such as performance standards or post-market surveillance—to ensure safety and effectiveness. Examples include custom crowns, casting alloys, and temporary restorations.

What are some examples of BEGO’s dental devices that appear in regulatory listings?

Examples of BEGO’s devices listed in regulatory databases include polymer crown systems like VarseoSmile TriniQ and Crown plus, resin-based temporary crowns and bridges, resin artificial teeth, and dental brazing alloys such as Wirobond 280 and Wirobond C. These products are authorised through pathways like 510(k) clearance or UDI registration.

Are BEGO’s devices authorised through any other regulatory pathways besides FDA 510(k) or UDI?

Based on the provided data, BEGO’s devices are only referenced in the FDA’s 510(k) clearance and UDI system registries in the United States. No other regulatory bodies or jurisdictions (e.g., EU MDR, international registries) are mentioned, so authorisation appears limited to U.S. FDA pathways for Class II devices.

AI-generated from registry data and not verified by a human reviewer.

Information

Country
US
Address
—
Website
bego.com
LinkedIn
—
Facebook
—
Phone
+4942120280
PRRC Contact
—
EUDAMED SRN
—
FDA FEI Number
—
DUNS Number
316483072

Catalogue (146)

Page 2 of 3
DeviceModel / ReferenceRegistriesClassStatus
Final Crown SRI0205046
FDA UDI
Class IIUnknown
Wiron light 50270
FDA UDI
Class IIActive
VarseoSmile Temp 41026US
FDA UDI
Class IIActive
VarseoSmile Temp 41024US
FDA UDI
Class IIActive
Bio PontoStar XL 61140
FDA UDI
Class IIActive
Final Crown SRI0205041
FDA UDI
Class IIUnknown
VarseoSmile Temp 41102US
FDA UDI
Class IIActive
WIRONIUM plus 50190
FDA UDI
Class IIActive
VarseoSmile TriniQ 41179US
FDA UDI
Class IIActive
Permanent Crown A3 FLPCA301US
FDA UDI
Class IIActive
SprintRay Crown SRI0205042
FDA UDI
Class IIActive
Mediloy M-Co 50951
FDA UDI
Class IIActive
VarseoSmile Teeth 41147US
FDA UDI
Class IIActive
VarseoSmile TriniQ 41173US
FDA UDI
Class IIActive
Wiron 99 50226
FDA UDI
Class IIActive
Temporary CB BL FLTCBL01US
FDA UDI
Class IIActive
Wiroweld NC 50006
FDA UDI
Class IIUnknown
VarseoSmile Temp 41023US
FDA UDI
Class IIActive
VarseoSmile TriniQ 41175US
FDA UDI
Class IIActive
VarseoSmile TriniQ 41188US
FDA UDI
Class IIActive
VarseoSmile Teeth 41157US
FDA UDI
Class IIActive
VarseoSmile TriniQ 41182US
FDA UDI
Class IIActive
Temporary CB A2 FLTCA201US
FDA UDI
Class IIActive
VarseoSmile Crown plus 41119US
FDA UDI
Class IIActive
Mediloy M-Ti4 50572
FDA UDI
Class IIActive
Mediloy M-Co 50956
FDA UDI
Class IIActive
Mediloy M-Co 50940
FDA UDI
Class IIActive
SprintRay Crown SRI0205045
FDA UDI
Class IIActive
Final Crown SRI0205042
FDA UDI
Class IIUnknown
VarseoSmile TriniQ 41184US
FDA UDI
Class IIActive
ECO d’OR 61112
FDA UDI
Class IIActive
Final Crown SRI0205043
FDA UDI
Class IIUnknown
VarseoSmile TriniQ BGTQA201
FDA UDI
Class IIActive
AuroLloyd M 61054
FDA UDI
Class IIActive
VarseoSmile TriniQ 41178US
FDA UDI
Class IIActive
VarseoSmile TriniQ 41186US
FDA UDI
Class IIActive
Final Crown SRI0205044
FDA UDI
Class IIUnknown
Mediloy M-Ti4 50574
FDA UDI
Class IIActive
Wironit 50030
FDA UDI
Class IIActive
Wironium RP 50530
FDA UDI
Class IIActive
Wiron light 50272
FDA UDI
Class IIActive
VarseoSmile TriniQ 41176US
FDA UDI
Class IIActive
Mediloy M-Co 50954
FDA UDI
Class IIActive
VarseoSmile Teeth 41146US
FDA UDI
Class IIActive
SprintRay Crown SRI0205044
FDA UDI
Class IIActive
SprintRay Crown SRI0205046
FDA UDI
Class IIActive
VarseoSmile Crown plus 41123US
FDA UDI
Class IIActive
Mediloy M-Co 50953
FDA UDI
Class IIActive
Final Crown SRI0205045
FDA UDI
Class IIUnknown
Mediloy M-Ti5 50596
FDA UDI
Class IIActive

Related Companies

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Authorities

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FDA Establishments (1)

Establishments registered with the FDA under this company group, matched by name.

  • Bego Bremer Goldschlaegerei Wilh. Herbst Gmbh & Co. Kg BREMEN · DE FEI 3002806467