Is this your brand? Sign in to claim ownership.
Sign in to claim this brandVOCO 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
- voco.de
- —
- —
- [email protected]
- Phone
- 999-999-9999
- PRRC Contact
- —
- EUDAMED SRN
- DE-MF-000008601
- FDA FEI Number
- 3002718942
- DUNS Number
- 316699578
Catalogue (880)
Page 10 of 18| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Grandio SO Flow | 2744 | EUDAMEDFDA UDI | Class II | Active |
| Grandio | 1853 | EUDAMEDFDA UDI | Class II | Active |
| Ionolux AC | 2122 | FDA UDI | Class II | Active |
| GrandioSO 4U | 6296 | FDA UDI | Class II | Active |
| V-Posil | 2564 | FDA UDI | Class II | Active |
| Admira Fusion | 2783 | EUDAMEDFDA UDI | Class II | Active |
| V-Print DT | 6905 | FDA UDI | Class II | Active |
| GrandioSO 4U | 6284 | FDA UDI | Class II | Active |
| Ionolux | 1991 | EUDAMEDFDA UDI | Class II | Active |
| Grandio blocs | 6162 | EUDAMEDFDA UDI | Class II | Active |
| V-Print splint | 6044 | FDA UDI | U | Active |
| Application cannulae | 2146 | EUDAMEDFDA UDI | Class I | Active |
| Structur 3 | 2507 | EUDAMEDFDA UDI | Class II | Active |
| Individo Lux | 2403 | FDA UDI | Class I | Active |
| BrackFix | 1208 | FDA UDI | Class II | Active |
| VOCO Profluorid Varnish | 2241 | EUDAMEDFDA UDI | Class II | Active |
| Admira Fusion 5 | 6230 | FDA UDI | Class II | Active |
| GrandioSO 4U | 6298 | FDA UDI | Class II | Active |
| Admira Fusion | 2798 | EUDAMEDFDA UDI | Class II | Active |
| Grandio SO Flow | 2726 | EUDAMEDFDA UDI | Class II | Active |
| Admira Flow | 2494 | FDA UDI | Class II | Active |
| Solobond Plus | 1049 | FDA UDI | Class II | Active |
| Grandio disc multicolor | 6216 | FDA UDI | Class II | Active |
| V-Posil | 2576 | FDA UDI | Class II | Active |
| GrandioSO 4U | 6282 | FDA UDI | Class II | Active |
| Grandio SO Flow | 2745 | FDA UDI | Class II | Active |
| Amaris Flow | 1946 | EUDAMEDFDA UDI | Class II | Active |
| Grandio Flow | 1865 | EUDAMEDFDA UDI | Class II | Active |
| Admira Fusion | 2763 | EUDAMEDFDA UDI | Class II | Active |
| Remin Pro | 2007 | FDA UDI | Class I | Active |
| Rebilda Form | 1407 | FDA UDI | Class I | Active |
| VOCO Ionofil Molar AC Quick | 1630 | FDA UDI | Class II | Active |
| Grandio blocs | 6004 | EUDAMEDFDA UDI | Class II | Active |
| Admira | 2421 | EUDAMEDFDA UDI | Class II | Active |
| Rebilda DC | 1404 | EUDAMEDFDA UDI | Class II | Active |
| Control Seal | 1303 | FDA UDI | Class II | Active |
| Ufi Gel SC | 2041 | EUDAMEDFDA UDI | Class II | Active |
| Caps Warmer | 9001 | FDA UDI | Class I | Active |
| Grandio blocs | 6159 | EUDAMEDFDA UDI | Class II | Active |
| Grandio disc multicolor | 6248 | EUDAMEDFDA UDI | Class II | Active |
| CediTEC DT | 6086 | EUDAMEDFDA UDI | Class II | Active |
| Grandio SO Heavy Flow | 2684 | EUDAMEDFDA UDI | Class II | Active |
| Grandio disc | 6055 | FDA UDI | Class II | Active |
| Grandio blocs | 6171 | FDA UDI | Class II | Active |
| Twinky Star | 1683 | FDA UDI | Class II | Active |
| Provicol | 1075 | FDA UDI | Class II | Active |
| Futurabond M | 1353 | FDA UDI | Class II | Active |
| Grandio blocs | 6023 | EUDAMEDFDA UDI | Class II | Active |
| Amaris | 1954 | FDA UDI | Class II | Active |
| Admira Fusion | 2787 | EUDAMEDFDA UDI | Class II | Active |
Related Companies
Authorised Representatives
No authorised representatives on record.
Importers
Not available yet.
Notified Bodies
Not available yet.
Authorities
Not available yet.