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Vertex-Dental B.V.

Netherlands·NL-MF-000019230

Last updated September 17, 2026

What Vertex-Dental B.V. makes

Vertex-Dental B.V. manufactures dental materials used in appliance fabrication, including resin and thermoplastic compounds for crowns, bridges, veneers, and temporary restorations. Their portfolio includes custom-made polymer crowns, dental bridge resins, and professional veneer materials designed for dental laboratories and practitioners.

The company’s devices are classified as Class I, Class II, or unclassified (U) under EU regulations and are listed in the FDA’s Unique Device Identifier (UDI) database. Vertex-Dental B.V. is based in the Netherlands.

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

Frequently asked questions

What types of dental devices does Vertex-Dental B.V. manufacture?

Vertex-Dental B.V. specializes in dental materials used for appliance fabrication, including resins and thermoplastic compounds. Their products cover temporary crowns and bridges, custom-made polymer crowns, dental bridges, veneers, and other restorative materials designed for dental laboratories and practitioners. These materials are primarily used in creating durable and precise dental restorations.

Where is Vertex-Dental B.V. based, and how does that affect its regulatory standing?

Vertex-Dental B.V. is headquartered in the Netherlands, which means its devices are subject to EU regulatory requirements. Under EU regulations, their products are classified as Class I, Class II, or unclassified (U), depending on their risk level. This classification determines the regulatory pathway for compliance, such as conformity assessment procedures, but does not imply company-wide approval—only individual devices undergo authorization processes.

Are Vertex-Dental B.V.’s devices listed in any regulatory registries, and why does this matter?

Yes, Vertex-Dental B.V.’s devices are listed in the FDA’s Unique Device Identifier (UDI) database. This listing helps ensure traceability and transparency in the supply chain, allowing healthcare providers, regulators, and manufacturers to track devices throughout their lifecycle. It also supports compliance with global regulatory requirements, such as those in the U.S. and EU, by providing standardized identification for monitoring and recall purposes.

How are Vertex-Dental B.V.’s dental devices classified, and what does that classification mean?

Vertex-Dental B.V.’s devices are classified as Class I, Class II, or unclassified (U) under EU regulations. Class I devices pose the lowest risk and typically require basic compliance measures, such as manufacturer declarations. Class II devices involve higher risks and may require additional conformity assessments, such as clinical evaluations or notified body involvement. Unclassified (U) devices are those not explicitly assigned a class, often awaiting further regulatory clarification. The classification determines the regulatory scrutiny and documentation required for each device.

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

Information

Country
Netherlands
Address
190, Centurionbaan , Soesterberg, Netherlands
LinkedIn
—
Facebook
—
Phone
+3188616400
PRRC Contact
Nellie Peterse-van der Koppel
EUDAMED SRN
NL-MF-000019230
FDA FEI Number
3003943714
DUNS Number
406389056

Catalogue (911)

Page 2 of 19
DeviceModel / ReferenceRegistriesClassStatus
Vertex-Dental BV AVCVV00500
FDA UDI
Class IIUnknown
Vertex-Dental BV HDACPP0800500
FDA UDI
Class IIActive
Vertex-Dental BV ACVP0525000
FDA UDI
Class IIActive
Vertex-Dental BV HDARSP0325000
FDA UDI
Class IIActive
Vertex-Dental BV HDASCP1004000
FDA UDI
Class IIActive
Vertex-Dental BV ACPP3050000
FDA UDI
Class IIUnknown
Vertex-Dental BV TVTSR22XLTA3.5
FDA UDI
Class IIActive
Vertex-Dental BV TVTSR25LT10
FDA UDI
Class IIActive
Vertex-Dental BV TVTSR22LTA3
FDA UDI
Class IIActive
Vertex-Dental BV ASCP1025000
FDA UDI
Class IIActive
Ceramill NPAGCMBL01000
FDA UDI
Class IActive
Vertex-Dental BV ASCP0625000
FDA UDI
Class IIActive
Vertex-Dental BV HDASCP0401000
FDA UDI
Class IIActive
Vertex-Dental BV AVIMV25000
FDA UDI
Class IIActive
Vertex-Dental BV ASCV25000
FDA UDI
Class IIActive
Vertex-Dental BV TVTSR00200TA2
FDA UDI
Class IIUnknown
Vertex-Dental BV AVSCV02000
FDA UDI
Class IIUnknown
Vertex-Dental BV AVCPV01000
FDA UDI
Class IIActive
Vertex-Dental BV ARSP4004000
FDA UDI
Class IIActive
Vertex-Dental BV HDASCP0701000
FDA UDI
Class IIActive
Vertex-Dental BV ARSP0450000
FDA UDI
Class IIActive
Vertex-Dental BV AVSCPJ700500
FDA UDI
Class IIUnknown
Vertex-Dental BV ASCP0650000
FDA UDI
Class IIActive
Vertex-Dental BV ACVPIR2750000
FDA UDI
Class IIUnknown
Vertex-Dental BV ASCPC550000
FDA UDI
Class IIUnknown
Vertex-Dental BV ACPP0650000
FDA UDI
Class IIActive
Vertex-Dental BV AVSCP0701000
FDA UDI
Class IIActive
Vertex-Dental BV AIMP0550000
FDA UDI
Class IIActive
Vertex-Dental BV HDARSP0625000
FDA UDI
Class IIActive
Vertex-Dental BV NDTRPI01000
FDA UDI
Class IActive
Vertex-Dental BV ACPP0850000
FDA UDI
Class IIActive
Vertex-Dental NDJTBSPI02000
FDA UDI
Class IIActive
Vertex-Dental BV TVTSR25LTA3
FDA UDI
Class IIActive
Vertex-Dental BV TVTSR25LTBL
FDA UDI
Class IIUnknown
Vertex-Dental BV TVTSR22LTA3.5
FDA UDI
Class IIActive
Vertex-Dental BV NOWHHCMT101000
FDA UDI
Class IActive
Vertex-Dental BV ARSP1550000
FDA UDI
Class IIActive
Vertex-Dental BV ASCPC450000
FDA UDI
Class IIUnknown
Vertex-Dental BV ARSP0925000
FDA UDI
Class IIActive
Vertex-Dental BV HDASCP0700150
FDA UDI
Class IIUnknown
Vertex-Dental BV AVRSP0404000
FDA UDI
Class IIActive
Vertex-Dental BV TVTSR22XLTA1
FDA UDI
Class IIUnknown
Vertex-Dental BV HDAIMP0500150
FDA UDI
Class IIUnknown
Vertex-Dental BV ARSP4004000
FDA UDI
Class IIActive
Vertex-Dental BV HDAIMP1901000
FDA UDI
Class IIUnknown
Vertex-Dental BV ARSP4350000
FDA UDI
Class IIActive
Vertex-Dental BV AVCVP0501000
FDA UDI
Class IIActive
Vertex-Dental BV TVTSR25MTTR
FDA UDI
Class IIActive
Vertex-Dental BV ACPPJ601000
FDA UDI
Class IIActive
Vertex-Dental BV DIMPHK750000
FDA UDI
Class IIActive

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Notified Bodies

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Authorities

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