xeyez
Netherlands NL-MF-000053485 Last updated 8 Jun 2026
- Devices
- 240
- Registries
- EUDAMED
- FDA recalls
- 0
Catalogue
ZeroRimVaria Ref ZRV57
ZeroRimCombo Ref ZRC51
FullRimVaria Ref FRV53
ZeroRimCombo Ref ZRC52
FullRimCombo Ref FRC44
ZeroRimPlastic Ref ZRP57
SemiRimVaria Ref SRV53
NeoRimVaria Ref NRV58
FullRimVaria Ref FRV50
SemiRimCombo Ref SRC48
SemiRimVaria Ref SRV54
NeoRimCombo Ref NRC44
SemiRimCombo Ref SRC47
NeoRimPlastic Ref NRP46
FullRimVaria Ref FRV56
FullRimVaria Ref FRV46
NeoRimCombo Ref NRC56
NeoRimCombo Ref NRC49
SemiRimMetal Ref SRM53
NeoRimPlastic Ref NRP47
ZeroRimCombo Ref ZRC44
SemiRimVaria Ref SRV57
ZeroRimMetal Ref ZRM53
FullRimCombo Ref FRC54
SemiRimPlastic Ref SRP55
NeoRimPlastic Ref NRP54
SemiRimVaria Ref SRV50
SemiRimPlastic Ref SRP46
ZeroRimPlastic Ref ZRP49
SemiRimCombo Ref SRC55
NeoRimPlastic Ref NRP51
ZeroRimMetal Ref ZRM44
NeoRimCombo Ref NRC46
NeoRimCombo Ref NRC55
ZeroRimVaria Ref ZRV53
FullRimMetal Ref FRM49
SemiRimCombo Ref SRC51
ZeroRimMetal Ref ZRM51
ZeroRimCombo Ref ZRC54
FullRimPlastic Ref FRP56
ZeroRimCombo Ref ZRC53
ZeroRimVaria Ref ZRV55
NeoRimCombo Ref NRC54
FullRimPlastic Ref FRP50
NeoRimCombo Ref NRC53
ZeroRimCombo Ref ZRC58
SemiRimPlastic Ref SRP58
NeoRimMetal Ref NRM58
NeoRimMetal Ref NRM48
NeoRimCombo Ref NRC50
Showing 51-100 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