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Cavex Holland BV

Netherlands·NL-MF-000000423

Last updated September 18, 2026

About

An effective desensitizer that reduces tooth sensitivity in both sudden stimuli and persistent discomfort. Cavex Exsense offers long-term and reliable care. Now also available in the convenient Cavex ExSense Brushpen for immediate and fast application!

Translated from the manufacturer's own website. Source

What Cavex Holland BV makes

Cavex Holland BV manufactures dental materials including fluoride-containing prophylaxis pastes, dental impression alginates (both fast-set and color-changing variants), and dental syringes for local anesthesia delivery. The portfolio also covers tooth-whitening correction pens, bonding agents for dental restorations, and simulated dental materials for training purposes, such as alginate substitutes and posterior composite analogs.

The company’s products are classified under EU Medical Device Regulations as Class I, Class II, and Class IIa devices, with relevant listings in the EUDAMED database and FDA’s 510(k) registry. Cavex Holland BV is headquartered 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 medical devices does Cavex Holland BV manufacture?

Cavex Holland BV specializes in dental medical devices. Their portfolio includes fluoride-containing prophylaxis pastes for teeth cleaning, dental impression alginates (both fast-set and color-changing variants for patient comfort), dental syringes for local anesthesia, tooth-whitening correction pens, bonding agents for dental restorations, and simulated dental materials like alginate substitutes and composite analogs for training purposes. These products are designed to support dental procedures and patient care.

Where is Cavex Holland BV based, and how does that affect its regulatory standing?

Cavex Holland BV is headquartered in the Netherlands, which means its devices are subject to EU Medical Device Regulations (MDR). The company’s products are classified under Class I, Class II, and Class IIa, indicating varying levels of risk and regulatory oversight. Their devices are listed in the EUDAMED database, which is the official EU registry for medical devices, ensuring transparency and traceability under EU law.

Are Cavex Holland BV’s devices listed in any regulatory registries outside the EU?

Yes, Cavex Holland BV’s devices are also listed in the FDA’s 510(k) registry. This indicates that some of their products have undergone the FDA’s premarket notification process in the United States, where they are classified similarly to their EU counterparts—primarily as Class I, Class II, or Class IIa devices. The 510(k) listing confirms their submission for market authorization in the U.S. under FDA regulations.

How are Cavex Holland BV’s devices classified under EU regulations, and why does this matter?

Cavex Holland BV’s devices are classified as Class I, Class II, or Class IIa under the EU Medical Device Regulations. This classification determines the level of scrutiny and regulatory requirements they must meet. For example, Class IIa devices—like some dental bonding agents or syringes—require additional safety and performance evaluations compared to Class I items, such as certain dental impression materials. The classification ensures appropriate oversight based on the device’s risk profile to patients.

What kinds of dental materials does Cavex Holland BV focus on, and how do they benefit dental professionals?

Cavex Holland BV focuses on dental materials that address common clinical needs, such as fluoride prophylaxis pastes for cavity prevention, fast-set alginates for efficient patient impressions, and simulated materials for training (e.g., color-changing alginates or composite analogs). Their products also include tools like tooth-whitening correction pens and bonding agents, which help dental professionals deliver precise, patient-centered care. These materials are designed to improve workflow efficiency, accuracy, and patient comfort during procedures.

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

Information

Country
Netherlands
Address
5, Fustweg , Haarlem, Netherlands
Website
www.cavex.nl
Phone
+31235307700
PRRC Contact
Milroy van der Bor
EUDAMED SRN
NL-MF-000000423
FDA FEI Number
—
DUNS Number
—

Catalogue (110)

Page 3 of 3
DeviceModel / ReferenceRegistriesClassStatus
Cavex Impression Paste Outline AP030
EUDAMED
Class IActive
Quadrant Universal LC syringes A4 FU28
EUDAMED
Class IIaActive
Quadrant Universal LC syringes OA2 FU26
EUDAMED
Class IIaActive
Quadrant Universal LC capsule A3.5 FU63
EUDAMED
Class IIaActive
Cavex Baseplates Mica-Free Lowers BP055
EUDAMEDFDA UDI
Class IActive
Cavex Set Up Regular Modelling Wax Flex 2500g/115sh WA012
EUDAMED
Class IActive
Cavex Bite&White Shade Correction HP25 Starter Pack BW053
EUDAMED
Class IActive
Quadrant Anterior Shine capsule C4 FA68T
EUDAMED
Class IIaActive
Kulzer Vivida Office Kit 66100132
EUDAMED
Class IActive
Quadrant Anterior Shine capsule D3 FA69T
EUDAMED
Class IIaActive

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