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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 3 of 3
DeviceModel / ReferenceRegistriesClassStatus
VarseoSmile TriniQ 41189US
FDA UDI
Class IIActive
Mediloy M-Ti5 50592
FDA UDI
Class IIActive
VarseoSmile Crown plus 41122US
FDA UDI
Class IIActive
Temporary CB B1 FLTCB101US
FDA UDI
Class IIActive
VarseoSmile Crown plus 41118US
FDA UDI
Class IIActive
SprintRay Crown SRI0205041
FDA UDI
Class IIActive
VarseoSmile Crown plus 41121US
FDA UDI
Class IIActive
VarseoSmile Temp 41103US
FDA UDI
Class IIActive
SprintRay Crown SRI0205040
FDA UDI
Class IIActive
Mediloy M-Ti5 50593
FDA UDI
Class IIActive
VarseoSmile Crown plus 41112US
FDA UDI
Class IIActive
Wirobond SG 50128
FDA UDI
Class IIActive
VarseoSmile TriniQ BGTQB101
FDA UDI
Class IIActive
VarseoSmile Crown plus 41113US
FDA UDI
Class IIActive
VarseoSmile TriniQ 41177US
FDA UDI
Class IIActive
Mediloy M-Ti5 50595
FDA UDI
Class IIActive
Mediloy M-Ti5 50591
FDA UDI
Class IIActive
VarseoSmile Teeth 41144US
FDA UDI
Class IIActive
VarseoSmile Teeth 41149US
FDA UDI
Class IIActive
VarseoSmile Crown plus 41120US
FDA UDI
Class IIActive
PontoLloyd P 61087
FDA UDI
Class IIActive
Wirobond C 50115
FDA UDI
Class IIActive
Temporary CB A3 FLTCA301US
FDA UDI
Class IIActive
Wiroweld 50005
FDA UDI
Class IIActive
Temporary CB C2 FLTCC201US
FDA UDI
Class IIActive
VarseoSmile Crown plus 41124US
FDA UDI
Class IIActive
BegoStar ECO 61121
FDA UDI
Class IIActive
Mediloy M-Ti4 50575
FDA UDI
Class IIActive
Kobalt-Chrom-Lot 52520
FDA UDI
Class IIActive
Mediloy M-Ti4 50577
FDA UDI
Class IIActive
BegoCer G 61097
FDA UDI
Class IIActive
Mediloy S-Co 50551
FDA UDI
Class IIActive
Mediloy M-Ti4 50573
FDA UDI
Class IIActive
VarseoSmile Teeth 41145US
FDA UDI
Class IIActive
Wirobond 280 50135
FDA UDI
Class IIActive
Permanent Crown A2 FLPCA201US
FDA UDI
Class IIActive
Wironit LA 50100
FDA UDI
Class IIActive
Wirobond C+ 50512
FDA UDI
Class IIActive
Mediloy M-Ti5 50594
FDA UDI
Class IIActive
Bece Press K090434
FDA 510(k)
Class IIActive
Bece Cad Zirkon Ht+ K132102
FDA 510(k)
Class IIActive
VarseoSmile Temp K193553
FDA 510(k)
Class IIActive
Begopal+ K123929
FDA 510(k)
Class IIActive
Begopal 300 K983081
FDA 510(k)
Class IIActive
VarseoSmile TriniQ K233596
FDA 510(k)
Class IIActive
VarseoSmile Crown plus K201668
FDA 510(k)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