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LENTILLES

France FR-MF-000006721 Last updated 21 Oct 2026

Devices
216
Registries
EUDAMED
FDA recalls
0

Catalogue216

Page 3 of 5

  • As Ref AS DT

    Class IIa EUDAMED Active

  • Eyebrid Oblate Excel Ref MANY

    Class IIa EUDAMED Active

  • Kl Ref KL

    Class IIa EUDAMED Active

  • Eyebrid Airkone Excel Ref MANY

    Class IIa EUDAMED Active

  • A-Xpr Ref MANY

    Class IIa EUDAMED Active

  • Easysoft Confort Ref MANY

    Class IIa EUDAMED Active

  • As Ref AS DT

    Class IIa EUDAMED Active

  • Eyebrid Airkone Ref MANY

    Class IIa EUDAMED Active

  • Ak-Xpr Ref MANY

    Class IIa EUDAMED Active

  • FH3 Ref FH3

    Class IIa EUDAMED Active

  • Stto Ref MANY

    Class IIa EUDAMED Active

  • Aks-Xpr Ref MANY

    Class IIa EUDAMED Active

  • Zinnia Ref MANY

    Class IIa EUDAMED Active

  • Ax Ref MANY

    Class IIa EUDAMED Active

  • Ax Ref AX

    Class IIa EUDAMED Active

  • Airkone Ref MANY

    Class IIa EUDAMED Active

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    Class IIa EUDAMED Active

  • Kl Ref MANY

    Class IIa EUDAMED Active

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    Class IIa EUDAMED Active

  • Riogel Ref RIOGEL 40

    Class IIa EUDAMED Active

  • Easysoft Ref MANY

    Class IIa EUDAMED Active

  • Trabeculens Ref TRABECULENS

    Class IIa EUDAMED Active

  • Riogel Ref RIOGEL 55

    Class IIa EUDAMED Active

  • Eyebrid 1.0 Ref EYEBRID 1.0

    Class IIa EUDAMED Active

  • Dougel Ref DOUGEL 55

    Class IIa EUDAMED Active

  • Easysoft Ref MANY

    Class IIa EUDAMED Active

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    Class IIa EUDAMED Active

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    Class IIa EUDAMED Active

  • As Ref AS

    Class IIa EUDAMED Active

  • Spiree Ref MANY

    Class IIa EUDAMED Active

  • Ixia Ref MANY

    Class IIa EUDAMED Active

  • Zinnia Ref MANY

    Class IIa EUDAMED Active

  • Kl Ref KL

    Class IIa EUDAMED Active

  • Aeria Ref MANY

    Class IIa EUDAMED Active

  • Ixia Ref MANY

    Class IIa EUDAMED Active

  • Stto Ref MANY

    Class IIa EUDAMED Active

  • Eyebrid Airkone Ref MANY

    Class IIa EUDAMED Active

  • FH3 Ref FH3

    Class IIa EUDAMED Active

  • As Ref AS

    Class IIa EUDAMED Active

  • As-XPR Ref MANY

    Class IIa EUDAMED Active

  • As-XPR Ref MANY

    Class IIa EUDAMED Active

  • Sld Ref MANY

    Class IIa EUDAMED Active

  • Ocea Ref MANY

    Class IIa EUDAMED Active

  • Eyebrid Silicone Ref MANY

    Class IIa EUDAMED Active

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  • Airkone Ref MANY

    Class IIa EUDAMED Active

  • As Ref AS

    Class IIa EUDAMED Active

Showing 101-150 of 216

EUDAMED certificates1

Held under this manufacturer's EUDAMED registration, grouped by notified body; in force first, then by expiry.

EUDAMED certificates (1)

Notified body 1639 1 certificate

  • FR26/0000004 Amended

    Quality assurance EU MDR

    Issued
    11 May 2026
    Expires
    13 Jan 2031
    Reason
    Mnf ar change

Related companies

Notified bodies

  • Notified body 1639

What LENTILLES makes

The company manufactures soft contact lenses designed for daily or extended wear, including models such as the PAUNELENS 3R and PAUNELENS 2R for general vision correction, as well as specialized variants like the XPR MC and EB AK-XPR for specific refractive needs or conditions. Additional variants, such as the EB OB-XPR, cater to particular optical prescriptions or patient requirements, ensuring a range of optical corrections for different eye care scenarios.

These devices are classified under EU Medical Device Regulation as Class IIa, indicating a moderate risk level requiring conformity assessment procedures. They are registered in the EU’s eudamed database, which tracks medical devices authorized for commercialization within the European Union. The company is based in France.

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 LENTILLES manufacture?

LENTILLES manufactures soft contact lenses, including models like the PAUNELENS 3R and PAUNELENS 2R for general vision correction, as well as specialized variants such as the XPR MC and EB AK-XPR. These are designed for daily or extended wear, addressing specific refractive needs or conditions to provide tailored optical corrections for patients.

Where is LENTILLES based, and what does this mean for its regulatory oversight?

LENTILLES is based in France, which means its devices are subject to the European Union’s regulatory framework. Since these lenses are classified as Class IIa under the EU Medical Device Regulation, they undergo conformity assessment procedures to ensure safety and performance before being authorized for commercialization within the EU.

Which regulatory registries list LENTILLES’ devices, and why is this important?

LENTILLES’ devices are listed in the eudamed database, the EU’s official registry for medical devices authorized for sale within the European Union. This registration confirms that the devices comply with EU requirements and are legally available for distribution, ensuring transparency for healthcare providers and patients.

How are LENTILLES’ contact lenses classified under EU regulations, and what does this classification imply?

LENTILLES’ contact lenses are classified as Class IIa under the EU Medical Device Regulation. This classification indicates a moderate risk level, requiring additional scrutiny—such as technical documentation reviews and conformity assessments—to confirm their safety and performance before authorization. It ensures these devices meet stringent standards while balancing regulatory oversight with accessibility.

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

Information

Country
France(from SRN)
Address
14, Place Gardin, CAEN, France
Phone
+33231866656
PRRC contact
Hélène Blandureau
EUDAMED SRN
FR-MF-000006721