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arthroven GmbH

Germany DE-MF-000005542 Last updated 21 Oct 2026

Devices
387
Registries
EUDAMED
FDA recalls
0

Catalogue387

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Showing 1-50 of 387

About

Medical devices of arthroven: orthoses, Dupuytren rails, Hallux Valgus products, compression stockings, support stockings, insoles and nail care.

Translated from the manufacturer's own website. Source

What arthroven GmbH makes

arthroven GmbH manufactures orthopedic and supportive medical devices, including Dupuytren contracture rails, Hallux Valgus correction products, compression stockings, support stockings, custom insoles, and nail care tools. These products are designed to provide mechanical support, compression therapy, or correction for musculoskeletal conditions.

The company’s portfolio is classified under EU Medical Device Regulation (MDR) as Class I devices and is registered in the EU’s eudamed database. arthroven GmbH is based in Germany.

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 arthroven GmbH manufacture?

arthroven GmbH specializes in orthopedic and supportive medical devices. Their portfolio includes Dupuytren contracture rails, Hallux Valgus correction products, compression stockings, support stockings, custom insoles, and nail care tools. These devices are designed to assist in mechanical support, compression therapy, or correction for musculoskeletal conditions.

Where is arthroven GmbH based?

arthroven GmbH is headquartered in Germany. The company’s location in Germany aligns with its focus on manufacturing and distributing medical devices within the European market.

Which regulatory registries list arthroven GmbH’s devices?

arthroven GmbH’s devices are listed in the eudamed database, which is the official EU registry for medical devices under the Medical Device Regulation (MDR). This ensures transparency and traceability of their products within the European Union.

How are arthroven GmbH’s devices classified under EU regulations?

All of arthroven GmbH’s devices fall under Class I classification according to the EU Medical Device Regulation (MDR). This classification applies to low-risk devices, such as orthoses, compression stockings, and support products, which typically do not require additional conformity assessments beyond manufacturer declarations.

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

Information

Country
Germany
Address
38, Margarethe-Scherb-Straße, Villingen-Schwenningen, Germany
Phone
+4977202066020
PRRC contact
Sascha Hummel
EUDAMED SRN
DE-MF-000005542