Is this your brand? Sign in to claim ownership.

Sign in to claim this brand

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 1 of 3
DeviceModel / ReferenceRegistriesClassStatus
VarseoSmile TriniQ 41181US
FDA UDI
Class IIActive
Wirobond 280 50134
FDA UDI
Class IIActive
VarseoSmile Crown plus 41114US
FDA UDI
Class IIActive
SprintRay Crown SRI0205054
FDA UDI
Class IIActive
VarseoSmile Crown plus 41111US
FDA UDI
Class IIActive
Mediloy M-Co 50955
FDA UDI
Class IIActive
VarseoSmile TriniQ 41180US
FDA UDI
Class IIActive
VarseoSmile Crown plus 41117US
FDA UDI
Class IIActive
VarseoSmile TriniQ 41172US
FDA UDI
Class IIActive
VarseoSmile Crown plus 41107US
FDA UDI
Class IIActive
Wirobond C 50116
FDA UDI
Class IIActive
Wirobond-Lot 52622
FDA UDI
Class IIActive
Mediloy RPD 50532US
FDA UDI
Class IIActive
VarseoSmile TriniQ 41174US
FDA UDI
Class IIActive
VarseoSmile TriniQ BGTQA301
FDA UDI
Class IIActive
Wironit extrahart 50060
FDA UDI
Class IIActive
VarseoSmile Crown plus 41108US
FDA UDI
Class IIActive
VarseoSmile Teeth 41156US
FDA UDI
Class IIActive
Mediloy M-Ti4 50576
FDA UDI
Class IIActive
BegoStar 61080
FDA UDI
Class IIActive
VarseoSmile TriniQ 41187US
FDA UDI
Class IIActive
Wiron-Lot 52625
FDA UDI
Class IIActive
BegoPal+ 61550
FDA UDI
Class IIUnknown
VarseoSmile Teeth 41148US
FDA UDI
Class IIActive
VarseoSmile Teeth 41155US
FDA UDI
Class IIActive
Mediloy M-Co 50952
FDA UDI
Class IIActive
VarseoSmile TriniQ 41183US
FDA UDI
Class IIActive
VarseoSmile Temp 41104US
FDA UDI
Class IIActive
Mediloy M-Ti4 50571
FDA UDI
Class IIActive
VarseoSmile Teeth 41154US
FDA UDI
Class IIActive
SprintRay Crown SRI0205043
FDA UDI
Class IIActive
VarseoSmile TriniQ 41185US
FDA UDI
Class IIActive
Mediloy M-Ti5 50597
FDA UDI
Class IIActive
Final Crown SRI0205040
FDA UDI
Class IIUnknown
VarseoSmile TriniQ 41170US
FDA UDI
Class IIActive
VarseoSmile TriniQ 41171US
FDA UDI
Class IIActive
VarseoSmile Temp 41022US
FDA UDI
Class IIActive
VarseoSmile Teeth 41159US
FDA UDI
Class IIActive
Mediloy M-Co 50957
FDA UDI
Class IIActive
BegoPal S 61086
FDA UDI
Class IIActive
WIRONIUM extrahart 50175
FDA UDI
Class IIActive
Wironium 50065
FDA UDI
Class IIActive
Permanent Crown C2 FLPCC201US
FDA UDI
Class IIActive
VarseoSmile Teeth 41158US
FDA UDI
Class IIActive
VarseoSmile Temp 41106US
FDA UDI
Class IIActive
CoCr DG1 50522US
FDA UDI
Class IIActive
BegoPal 300 61105
FDA UDI
Class IIActive
Permanent Crown B1 FLPCB101US
FDA UDI
Class IIActive
VarseoSmile Crown plus 41110US
FDA UDI
Class IIActive
Mediloy RPD 50532
FDA UDI
Class IIActive

Related Companies

Authorised Representatives

No authorised representatives on record.

Importers

Not available yet.

Notified Bodies

Not available yet.

Authorities

Not available yet.

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