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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 (685)

Page 9 of 14
DeviceModel / ReferenceRegistriesClassStatus
Bifix SE 1786
FDA UDI
Class IIActive
Registrado Scan 2038
FDA UDI
Class IIActive
Amaris 1942
FDA UDI
Class IIActive
Caps Warmer 9003
FDA UDI
Class IActive
VisCalor bulk 6066
FDA UDI
Class IIActive
Grandio SO 2601
FDA UDI
Class IIActive
Profluorid L 1592
FDA UDI
Class IIActive
Mixing tips 2186
EUDAMEDFDA UDI
Class IActive
Grandio SO Heavy Flow 2696
FDA UDI
Class IIActive
CleanJoy 6096
FDA UDI
Class IActive
GrandioSO 4U 6285
FDA UDI
Class IIActive
CediTEC DB 6197
FDA UDI
Class IIUnknown
Mixing spatula 2168
FDA UDI
Class IActive
Admira Protect 1652
FDA UDI
Class IIActive
Grandio 1814
EUDAMEDFDA UDI
Class IIActive
Grandio disc 6056
FDA UDI
Class IIActive
Solobond Plus 1044
FDA UDI
Class IIActive
Grandio blocs 6184
FDA UDI
Class IIActive
Rebilda Post GT 1972
EUDAMEDFDA UDI
Class IActive
IonoStar Plus 2544
FDA UDI
Class IIActive
Admira 2423
FDA UDI
Class IIActive
Grandio SO 2610
FDA UDI
Class IIActive
Curvy 2063
FDA UDI
Class IActive
V-Posil 2570
FDA UDI
Class IIActive
Admira Fusion x-base 2813
EUDAMEDFDA UDI
Class IIActive
Mixing tips 2203
FDA UDI
Class IActive
VisCalor Dispenser 9143
FDA UDI
Class IActive
Structur 3 2998
FDA UDI
Class IIActive
Grandio blocs 6168
FDA UDI
Class IIActive
Admira Fusion Flow 2820
FDA UDI
Class IIActive
Structur 2 1481
FDA UDI
Class IIActive
GrandioSO x-tra 2595
FDA UDI
Class IIActive
CleanJoy 6100
FDA UDI
Class IActive
IonoStar Molar 2524
FDA UDI
Class IIActive
Structur Premium 1715
FDA UDI
Class IIActive
Rebilda DC 1399
FDA UDI
Class IIActive
CleanJoy 6094
FDA UDI
Class IActive
Mixing tips 2189
EUDAMEDFDA UDI
Class IActive
Grandio SO Flow 2723
FDA UDI
Class IIActive
Admira 2426
FDA UDI
Class IIActive
Admira Fusion 2779
FDA UDI
Class IIActive
GrandioSO 4U 6294
FDA UDI
Class IIActive
CleanJoy 2093
FDA UDI
Class IActive
Ufi Gel SC 2029
FDA UDI
Class IIActive
Quick Up 1628
FDA UDI
Class IIActive
VisCalor 6113
FDA UDI
Class IIActive
Bifix QM 1219
EUDAMEDFDA UDI
Class IIActive
GrandioSO 4U 6289
FDA UDI
Class IIActive
VisCalor 6120
FDA UDI
Class IIActive
Admira 2430
FDA UDI
Class IIActive

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