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VOCO GmbH

Germany·DE-MF-000008601

Last updated September 17, 2026

What VOCO GmbH makes

VOCO GmbH manufactures dental materials including composite resins for restorations, temporary crowns and bridges, bonding agents for dentine, silicone impression materials, desensitizing coatings, glass ionomer cements, and tooth-whitening products. Their portfolio also includes dentifrices and specialized mixing nozzles for dental applications.

The company’s devices are classified under EU Medical Device Regulations as Class I, Class II, Class IIa, and Unclassified (U), with listings in the EUDAMED database and the FDA’s UDI system. VOCO GmbH is based in Germany.

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 VOCO GmbH primarily manufacture?

VOCO GmbH specializes in dental materials, including composite resins for fillings and restorations, temporary crowns and bridges, bonding agents for tooth preparation, silicone impression materials for molds, desensitizing coatings for teeth, glass ionomer cements for restorations, and tooth-whitening products. Their portfolio also covers dentifrices (toothpastes) and specialized mixing nozzles for dental applications. These products are designed to support restorative, preventive, and cosmetic dental procedures.

Where is VOCO GmbH based, and how does this affect its regulatory compliance?

VOCO GmbH is based in Germany, which means its devices must comply with the European Union’s Medical Device Regulations (MDR) or In Vitro Diagnostic Regulation (IVDR) depending on classification. Since the company’s devices are listed in the EUDAMED database, this indicates they are registered under EU regulatory requirements. The FDA’s UDI system listing further suggests their devices are also marketed in the U.S., where they must adhere to FDA regulations.

Which regulatory registries list VOCO GmbH’s devices, and why is this important?

VOCO GmbH’s devices are listed in EUDAMED, the European Union’s medical device registry, and the FDA’s UDI system, which tracks devices marketed in the U.S. Inclusion in these registries demonstrates compliance with respective regulatory bodies: EUDAMED confirms registration under EU MDR, while FDA UDI ensures traceability and transparency for U.S. market access. These listings help healthcare providers, regulators, and authorities verify the legitimacy and classification of the devices.

How are VOCO GmbH’s dental devices classified under EU regulations?

VOCO GmbH’s devices fall under Class I, Class II, Class IIa, and Unclassified (U) categories in the EU Medical Device Regulations. Classification depends on factors like risk level, intended use, and interaction with the body—for example, low-risk items like some dental coatings may qualify as Class I, while more complex restorative materials (e.g., composites or bonding agents) could be Class II or IIa due to their functional role in dental procedures. The classification determines regulatory requirements, such as clinical evaluations or conformity assessments.

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

Information

Country
Germany
Address
1-3, Anton-Flettner-Str., Cuxhaven, Germany
Website
www.voco.de
LinkedIn
—
Facebook
—
Phone
999-999-9999
PRRC Contact
Andreas Lawerenz
EUDAMED SRN
DE-MF-000008601
FDA FEI Number
3002718942
DUNS Number
316699578

Catalogue (679)

Page 4 of 14
DeviceModel / ReferenceRegistriesClassStatus
Grandio blocs 6029
FDA UDI
Class IIActive
Ufi Gel hard C 2217
FDA UDI
Class IIActive
VisCalor bulk 6063
FDA UDI
Class IActive
Grandio blocs 6009
FDA UDI
Class IIActive
Admira Fusion 2776
FDA UDI
Class IIActive
Amaris 1950
FDA UDI
Class IIActive
Rebilda Form 1408
FDA UDI
Class IActive
Grandio 1812
FDA UDI
Class IIActive
Structur CAD 6079
FDA UDI
Class IIActive
Grandio SO Heavy Flow 2688
FDA UDI
Class IIActive
Structur 3 2504
FDA UDI
Class IIActive
Remin Pro 2009
FDA UDI
Class IActive
Twinky Star 1688
FDA UDI
Class IIActive
Mixing tips 2202
EUDAMEDFDA UDI
Class IActive
V-Posil 2987
FDA UDI
Class IIActive
Grandio SO 2655
FDA UDI
Class IIActive
V-Posil 2574
FDA UDI
Class IIActive
VOCO Profluorid Varnish 2229
FDA UDI
Class IIActive
Amaris 1934
FDA UDI
Class IIActive
Grandio Flow 1897
FDA UDI
Class IIActive
Grandio SO Heavy Flow 2704
FDA UDI
Class IIActive
Grandio SO Heavy Flow 2693
FDA UDI
Class IIActive
Profluorid L 1590
FDA UDI
Class IIActive
Bifix Hybrid Abutment Cement 2413
FDA UDI
Class IIActive
Admira 2454
FDA UDI
Class IIActive
Structur 3 2518
FDA UDI
Class IIActive
Admira Flow 2492
FDA UDI
Class IIActive
Dimanto 2383
FDA UDI
Class IActive
Structur 2 1480
FDA UDI
Class IIActive
Ufi Gel SC 2047
FDA UDI
Class IIActive
Futurabond NR 1148
FDA UDI
Class IIActive
Grandio SO Inlay System 2642
FDA UDI
Class IIActive
Bifix Hybrid Abutment Cement 2411
FDA UDI
Class IIActive
Brush holder 2338
FDA UDI
Class IActive
GrandioSO x-tra 2596
FDA UDI
Class IIActive
Admira Fusion 2772
FDA UDI
Class IIActive
Pele Tim 2252
FDA UDI
Class IActive
Grandio Seal 1061
EUDAMEDFDA UDI
Class IIActive
V-Posil 2573
FDA UDI
Class IIActive
Admira Fusion Flow 2826
FDA UDI
Class IIActive
Grandio SO Heavy Flow 2691
FDA UDI
Class IIActive
Grandio blocs 6183
FDA UDI
Class IIActive
Admira Fusion x-tra 2808
FDA UDI
Class IIActive
Grandio SO 2646
FDA UDI
Class IIActive
Admira Fusion 5 6231
FDA UDI
Class IIActive
Futurabond NR 1153
FDA UDI
Class IIActive
VisCalor bulk 6062
FDA UDI
Class IActive
Dimanto 2380
FDA UDI
Class IActive
Intraoral tips 2141
EUDAMEDFDA UDI
Class IActive
GrandioSO x-tra 2719
FDA UDI
Class IIActive

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