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Feguramed GmbH

Germany·DE-MF-000019995

Last updated September 18, 2026

About

Feguramed presents on IDS.online - the leading trade fair and online platform for the dental industry, presenting manufacturers, products and services for dental professionals worldwide.

From the manufacturer's own website. Source

What Feguramed GmbH makes

Feguramed GmbH manufactures dental bonding materials and related products, including Combibond lot variants, Combibond GC 3, Combibond Laserschweißdraht, Combibond GG 2, Combibond BST Triumph, and Combilium BSM 5. The company also produces Fegura Bond Opakerpulver in various shades (weiß, A3, 5, dunkel-rosa) and MC-Bonder Keramikbonder for dental applications.

The devices manufactured by Feguramed GmbH are classified as Class IIa under the EU regulatory framework and are listed in the Eudamed database. The company is based in Germany (DE).

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

Frequently asked questions

What does Feguramed GmbH manufacture?

Feguramed GmbH manufactures dental bonding materials and related products, including Combibond lot variants such as Combibond Lot 1, Lot 2, and Lot 9, Combibond GC 3, Combibond Laserschweißdraht, Combibond GG 2, Combibond BST Triumph, and Combilium BSM 5. The company also produces Fegura Bond Opakerpulver in various shades including weiß, A3, 5, and dunkel-rosa, as well as MC-Bonder Keramikbonder for dental applications.

Where is Feguramed GmbH based?

Feguramed GmbH is based in Germany, as indicated by the country code DE in the provided data. The company’s location is specified within the device data under the COUNTRY field, confirming its establishment in Germany.

In which regulatory registry are Feguramed GmbH's devices listed?

Feguramed GmbH's devices are listed in the Eudamed database, which is the European Union’s medical device registry. This is explicitly stated in the LISTED IN field of the device data, confirming the company’s products are registered in Eudamed for regulatory transparency within the EU.

How are Feguramed GmbH's devices classified under EU regulations?

Feguramed GmbH's devices are classified as Class IIa under the EU regulatory framework. This classification is directly stated in the DEVICE CLASSES field of the provided data, indicating that the products fall under medium-risk category requiring conformity assessment but not the highest level of scrutiny.

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

Information

Country
Germany
Address
2, Jahnstraße, Buchen (Odenwald), Germany
LinkedIn
—
Facebook
—
Phone
+49 6281 52270
PRRC Contact
Maximilian Seefelder
EUDAMED SRN
DE-MF-000019995
FDA FEI Number
—
DUNS Number
—

Catalogue (21)

DeviceModel / ReferenceRegistriesClassStatus
Combibond Lot 2 1000 011
EUDAMED
Class IIaActive
Combibond Lot 1 1000 010
EUDAMED
Class IIaActive
Combibond Lot 9 1000 031
EUDAMED
Class IIaActive
Fegura Bond Opakerpulver weiß 2183
EUDAMED
Class IIaActive
Combibond GC 3 1000 003
EUDAMED
Class IIaActive
Combibond Laserschweißdraht 4085, 4090
EUDAMED
Class IIaActive
Combibond GG 2 1000 018
EUDAMED
Class IIaActive
Combilium BSM 5 2192
EUDAMED
Class IIaActive
Fegura Bond Opakerpulver A3, 5 2183-2
EUDAMED
Class IIaActive
MC-Bonder Keramikbonder 4010
EUDAMED
Class IIaActive
Fegura Bond Opakerpulver dunkel-rosa 2182-2
EUDAMED
Class IIaActive
Combibond BST Triumph 4030, 4035
EUDAMED
Class IIaActive
Combilium BSM 3 2191
EUDAMED
Class IIaActive
Combilium BSM 4 2190
EUDAMED
Class IIaActive
Combibond GC 4 1000 004
EUDAMED
Class IIaActive
Combibond GG 3 1000 019
EUDAMED
Class IIaActive
Combibond Lot 5 1000 014
EUDAMED
Class IIaActive
Fegura Bond Anmischflüssigkeit 2184
EUDAMED
Class IIaActive
Fegura Bond Opakerpulver rosa 2182
EUDAMED
Class IIaActive
Combibond SG 1 1000 023
EUDAMED
Class IIaActive
Combibond Lot 7 1000 029
EUDAMED
Class IIaActive

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