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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 3 of 14
DeviceModel / ReferenceRegistriesClassStatus
Admira 2431
FDA UDI
Class IIActive
Celalux 3 9996
FDA UDI
Class IIActive
GrandioSO Light Flow 2586
FDA UDI
Class IIActive
GrandioSO Light Flow 2593
FDA UDI
Class IIActive
VisCalor Dispenser 9146
FDA UDI
Class IActive
VisCalor 6117
FDA UDI
Class IIActive
Futurabond M 1350
FDA UDI
Class IIActive
Remin Pro 2005
FDA UDI
Class IActive
Structur 3 2516
FDA UDI
Class IIActive
Structur 2 1309
FDA UDI
Class IIActive
VOCO Profluorid Varnish 2226
FDA UDI
Class IIActive
IonoStar Molar 2524
FDA UDI
Class IIActive
Structur Premium 1714
FDA UDI
Class IIActive
Grandio Flow 1874
FDA UDI
Class IIActive
Rebilda Post 1773
FDA UDI
Class IActive
Grandio disc multicolor 6218
FDA UDI
Class IIActive
trifill instrument 2169
FDA UDI
Class IActive
Grandio Flow 1873
FDA UDI
Class IIActive
Structur 2 1485
FDA UDI
Class IIActive
Quick Up LC 1627
FDA UDI
Class IIActive
Admira Fusion 2760
FDA UDI
Class IIActive
Admira Fusion 2794
FDA UDI
Class IIActive
Grandio blocs 6173
FDA UDI
Class IIActive
GrandioSO 4U 6295
FDA UDI
Class IIActive
Admira Fusion 2752
FDA UDI
Class IIActive
Structur CAD 6073
FDA UDI
Class IIActive
Grandio 1830
FDA UDI
Class IIActive
BrackFix 1209
FDA UDI
Class IIActive
Admira Fusion 2791
FDA UDI
Class IIActive
Dispenser 9302
EUDAMEDFDA UDI
Class IActive
CleanJoy 2098
FDA UDI
Class IActive
IonoStar Plus 2547
FDA UDI
Class IIActive
GrandioSO Light Flow 2587
FDA UDI
Class IIActive
Grandio blocs 6158
FDA UDI
Class IIActive
CleanJoy 2100
FDA UDI
Class IActive
Admira Fusion 2792
FDA UDI
Class IIActive
Grandio SO 2667
FDA UDI
Class IIActive
Celalux III 9091
FDA UDI
Class IIActive
V-Print DT 6904
FDA UDI
Class IIActive
GrandioSO 4U 6290
FDA UDI
Class IIActive
Provicol 1078
FDA UDI
Class IIActive
Grandio SO Heavy Flow 2706
FDA UDI
Class IIActive
Dimanto 2382
FDA UDI
Class IActive
Grandio disc multicolor 6219
FDA UDI
Class IIActive
Admira 2429
FDA UDI
Class IIActive
Grandio SO Heavy Flow 2692
FDA UDI
Class IIActive
Admira Fusion 2784
FDA UDI
Class IIActive
Provicol QM 1109
FDA UDI
Class IIActive
V-Posil 2562
FDA UDI
Class IIActive
Grandio SO 2633
FDA UDI
Class IIActive

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