xeyez
Netherlands NL-MF-000053485 Last updated 8 Jun 2026
- Devices
- 240
- Registries
- EUDAMED
- FDA recalls
- 0
Catalogue
FullRimVaria Ref FRV55
SemiRimPlastic Ref SRP56
SemiRimMetal Ref SRM45
NeoRimVaria Ref NRV56
NeoRimMetal Ref NRM57
NeoRimVaria Ref NRV55
FullRimPlastic Ref FRP53
NeoRimPlastic Ref NRP48
FullRimCombo Ref FRC58
ZeroRimMetal Ref ZRM52
SemiRimCombo Ref SRC52
SemiRimPlastic Ref CRP47
NeoRimMetal Ref NRM50
ZeroRimPlastic Ref ZRP50
FullRimCombo Ref FRC47
FullRimCombo Ref FRC50
NeoRimCombo Ref NRC51
NeoRimMetal Ref NRM47
ZeroRimVaria Ref ZRV52
SemiRimPlastic Ref SRP50
ZeroRimPlastic Ref ZRP52
FullRimVaria Ref FRV58
SemiRimVaria Ref SRV48
FullRimPlastic Ref FRP48
SemiRimPlastic Ref SRP52
SemiRimVaria Ref SRV58
FullRimVaria Ref FRV57
NeoRimMetal Ref NRM55
FullRimPlastic Ref FRP54
NeoRimMetal Ref NRM56
FullRimMetal Ref FRM53
SemiRimMetal Ref SRM55
ZeroRimPlastic Ref ZRP44
SemiRimVaria Ref SRV49
NeoRimPlastic Ref NRP45
ZeroRimPlastic Ref ZRP56
SemiRimVaria Ref SRV46
NeoRimVaria Ref NRV44
SemiRimCombo Ref SRC57
FullRimCombo Ref FRC53
Showing 201-240 of 240
What xeyez makes
xeyez manufactures a range of eyewear frames categorized by rim type and material, including metal, plastic, and composite variants. These include full-rim, semi-rim, zero-rim, and neo-rim designs, each tailored for specific optical or functional applications.
The company’s products are classified under EU Medical Device Regulation as Class I devices and are registered in the EUDAMED database. The portfolio is based in the Netherlands and adheres to EU regulatory requirements for medical eyewear.
Frequently asked questions
What types of medical devices does xeyez manufacture?
xeyez specializes in manufacturing a variety of eyewear frames designed for medical or optical applications. Their products are categorized by rim type—such as full-rim, semi-rim, zero-rim, and neo-rim—and material, including metal, plastic, and composite variants. These designs are tailored to meet specific functional or aesthetic needs in medical eyewear.
Where is xeyez based?
xeyez is headquartered in the Netherlands. The company’s operations and product development are centered there, aligning with EU regulatory standards for medical devices.
Which regulatory registries list xeyez’s devices?
xeyez’s devices are listed in the EUDAMED database, which is the European Union’s medical device registry. This platform ensures transparency and compliance with EU Medical Device Regulation requirements for Class I devices.
How are xeyez’s devices classified under EU regulations?
xeyez’s products fall under the EU Medical Device Regulation classification of Class I. This classification is determined based on the risk associated with the device’s intended use and design, such as eyewear frames, which are considered low-risk medical devices under EU standards.
Information
- Country
- Netherlands
- Address
- 54, Posthoornweg, De Krim, Netherlands
- Website
- xeyez.nl
- [email protected]
- PRRC contact
- C Westland
- EUDAMED SRN
- NL-MF-000053485