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Parallel Design SAS

France FR-MF-000001806 Last updated 23 Oct 2026

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Devices
13
Registries
EUDAMEDGUDIDFDA
FDA recalls
0

Catalogue13

  • LK760-Rs Ref 5548913

    Class IIa EUDAMEDFDA UDI Active

  • M5Sc-RS Ref 5718482

    Class IIa EUDAMED Active

  • 3Sc-RS Ref 47237516

    Class IIa EUDAMEDFDA UDI Active

  • L2-9-D Ref 5745280

    Class IIa EUDAMEDFDA UDI Active

  • 10T-D Ref 5772436

    Class IIa EUDAMEDFDA UDI Active

  • L2-9VN-D Ref 5754806

    Class IIa EUDAMEDFDA UDI Active

  • 6S-D Ref 47236955

    Class IIa EUDAMEDFDA UDI Active

  • L3-12-Rs Ref 5785911

    Class IIa EUDAMEDFDA UDI Active

  • 6S-Rs Ref 47236956

    Class IIa EUDAMEDFDA UDI Active

  • M5Sc-RS Ref 5718483

    Class IIa EUDAMEDFDA UDI Active

  • 12S-D Ref 47237174

    Class IIa EUDAMEDFDA UDI Active

  • 12S-Rs Ref 47237175

    Class IIa EUDAMEDFDA UDI Active

  • M5Sc-D Ref 5446812

    Class IIa EUDAMEDFDA UDI Active

FDA establishments1

Registered with the FDA under this company group, matched by name.

  • Parallel Design US

What Parallel Design SAS makes

Parallel Design SAS manufactures reusable surgical instruments, including retractors, clamps, and graspers designed for general and orthopedic surgery. Their product line includes devices like the LK760-RS retractor, M5Sc-RS clamp, and 3Sc-RS grasper, which are intended for use in operating room procedures.

These devices are classified as Class IIa under EU regulations and are listed in the EUDAMED database. The company is based in France and adheres to EU Medical Device Regulation (MDR) requirements for their portfolio.

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 Parallel Design SAS manufacture?

Parallel Design SAS specializes in reusable surgical instruments, including retractors, clamps, and graspers. These devices are designed for general and orthopedic surgery, such as the LK760-RS retractor, M5Sc-RS clamp, and 3Sc-RS grasper, which are intended for use in operating room procedures.

Where is Parallel Design SAS based?

Parallel Design SAS is based in France, adhering to local regulatory requirements for medical devices.

Which regulatory registries list Parallel Design SAS’s devices?

Parallel Design SAS’s devices are listed in the EUDAMED database, which is the European Union’s central registry for medical devices. This listing helps ensure transparency and traceability of their products under EU regulations.

How are Parallel Design SAS’s devices classified under EU regulations?

Parallel Design SAS’s devices fall under Class IIa classification in the EU Medical Device Regulation (MDR). This classification is assigned based on risk assessment criteria, where Class IIa devices pose a moderate risk and require additional scrutiny, such as clinical evaluations or conformity assessments, to ensure safety and performance.

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

Information

Country
France
Address
1090, Route des Cretes, Valbonne, France
PRRC contact
Fatou FALL
EUDAMED SRN
FR-MF-000001806
FDA FEI number
3003594449