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ARTIQO GmbH

Germany·DE-MF-000007336

Last updated September 18, 2026

About

ARTIQO Endoprosthetics develops and distributes endoprosthetic products for the hip, knee and foot.

Translated from the manufacturer's own website. Source

What ARTIQO GmbH makes

ARTIQO GmbH manufactures orthopedic instrumentation and components for knee and hip endoprosthetics, including femoral and tibial positioning guides, trial implants, and alignment tools. Their products include modular trial components for femoral and tibial sizing, cortical sensors for intraoperative assessment, and specialized cutting blocks for bone preparation. Additional items cover angular adjustment adapters and customizable trial implants for left and right-sided applications.

The company’s portfolio spans Class I, Class IIa, and Class III medical devices under EU regulations, with all products registered in the EUDAMED database. The manufacturer is based in Germany and adheres to EU medical device directives and MDR compliance requirements for its orthopedic instrumentation and endoprosthetic components.

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 ARTIQO GmbH manufacture?

ARTIQO GmbH specializes in orthopedic instrumentation and components for knee and hip endoprosthetics. Their products include femoral and tibial positioning guides, trial implants for sizing and testing, cortical sensors for intraoperative bone assessment, cutting blocks for bone preparation, and angular adjustment adapters. These devices are designed to assist surgeons during joint replacement procedures, ensuring precise alignment and fit of prosthetic components.

Where is ARTIQO GmbH based, and what regulatory framework does it follow?

ARTIQO GmbH is based in Germany. The company develops and distributes medical devices that fall under EU medical device regulations, including Class I, Class IIa, and Class III classifications. All of its products are registered in the EUDAMED database, which is the official EU registry for medical devices, ensuring transparency and traceability in compliance with EU Medical Device Regulations (MDR).

Which regulatory registries list ARTIQO GmbH’s devices?

ARTIQO GmbH’s devices are listed in the EUDAMED database, which is the European Union’s central registry for medical devices. This registry is used to track device information, including manufacturer details, device classifications, and regulatory compliance under EU medical device laws. Listing in EUDAMED ensures visibility and adherence to transparency requirements for devices marketed within the EU.

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

ARTIQO GmbH’s devices are classified into three categories under EU medical device regulations: Class I (typically low-risk devices like simple orthopedic tools), Class IIa (moderate-risk devices such as trial implants and alignment guides), and Class III (high-risk devices like certain endoprosthetic components requiring stringent scrutiny). Classification depends on factors like intended use, risk to patients, and the degree of intervention, with higher classes requiring more rigorous pre-market evaluation and post-market surveillance.

What kinds of endoprosthetic components does ARTIQO GmbH provide for hip and knee surgeries?

ARTIQO GmbH provides a range of modular trial components for hip and knee endoprosthetics, including femoral and tibial positioning guides for intraoperative alignment, trial implants (e.g., left/right femoral probes) to test sizing and fit, cutting blocks for precise bone preparation, and cortical sensors to assess bone quality during surgery. Their portfolio also includes angular adjustment adapters and customizable trial inlays to accommodate anatomical variations, ensuring tailored solutions for surgical planning.

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

Information

Country
Germany
Address
57, Hans-Böckler-Straße, Lüdinghausen, Germany
Website
www.artiqo.de
LinkedIn
—
Facebook
—
Phone
+49 2591-8931500
PRRC Contact
Mario Frank
EUDAMED SRN
DE-MF-000007336
FDA FEI Number
—
DUNS Number
—

Catalogue (238)

Page 3 of 5
DeviceModel / ReferenceRegistriesClassStatus
BSM Aufnahme 9211610-04
EUDAMED
Class IActive
4-motion® Tibiagrößenlehre PSA Gr. 10 9210920
EUDAMED
Class IIaActive
4-motion® Bandspanner 9211600
EUDAMED
Class IActive
4-motion® Tibia-Größenlehre Gr.7 9210907
EUDAMED
Class IIaActive
4-motion® knee inlay 7411-1009
EUDAMED
Class IIIActive
4-motion® knee inlay 7401-0106
EUDAMED
Class IIIActive
A2® short stem 311301
EUDAMED
Class IIIActive
4-motion® knee inlay 7401-0912
EUDAMED
Class IIIActive
4-motion® knee inlay 7411-0812
EUDAMED
Class IIIActive
4-motion® knee tibial component 4601-L003
EUDAMED
Class IIIActive
4-motion® knee tibial component 4631-L004
EUDAMED
Class IIIActive
4-motion® knee tibial component 3631-L004
EUDAMED
Class IIIActive
4-motion® knee inlay 7411-0315
EUDAMED
Class IIIActive
4-motion® knee inlay 7401-1006
EUDAMED
Class IIIActive
A2® short stem 411308
EUDAMED
Class IIIActive
4-motion® knee inlay 7411-0510
EUDAMED
Class IIIActive
4-motion® knee tibial component 4601-L009
EUDAMED
Class IIIActive
A2® short stem 311107
EUDAMED
Class IIIActive
4-motion® knee inlay 7401-0610
EUDAMED
Class IIIActive
4-motion® knee inlay 7411-0206
EUDAMED
Class IIIActive
4-motion® knee femoral component 4811-LW06
EUDAMED
Class IIIActive
A2® short stem 311303
EUDAMED
Class IIIActive
4-motion® knee inlay 7411-0811
EUDAMED
Class IIIActive
4-motion® knee patellar component 4101-0829
EUDAMED
Class IIIActive
4-motion® knee tibial component 3631-R001
EUDAMED
Class IIIActive
4-motion® knee inlay 7401-1010
EUDAMED
Class IIIActive
4-motion® knee inlay 7401-0210
EUDAMED
Class IIIActive
4-motion® knee inlay 7411-0910
EUDAMED
Class IIIActive
ELEC®plus femoral head 726322
EUDAMED
Class IIIActive
4-motion® knee inlay 7401-0906
EUDAMED
Class IIIActive
A2® short stem 311109
EUDAMED
Class IIIActive
4-motion® knee inlay 7401-0310
EUDAMED
Class IIIActive
4-motion® knee inlay 7411-0915
EUDAMED
Class IIIActive
4-motion® knee tibial component 4631-R005
EUDAMED
Class IIIActive
A2® short stem 311209
EUDAMED
Class IIIActive
ELEC®plus Revision - femoral head 727324
EUDAMED
Class IIIActive
4-motion® knee tibial component 4601-L010
EUDAMED
Class IIIActive
A2® short stem 311105
EUDAMED
Class IIIActive
4-motion® knee inlay 7411-0610
EUDAMED
Class IIIActive
4-motion® knee inlay 4-motion® knee inlay
EUDAMED
Class IIIActive
4-motion® knee inlay 7411-0813
EUDAMED
Class IIIActive
4-motion® knee inlay 7411-0115
EUDAMED
Class IIIActive
4-motion® knee inlay 7401-0806
EUDAMED
Class IIIActive
4-motion® knee femoral component 4801-RS05
EUDAMED
Class IIIActive
ELEC®plus femoral head 726282
EUDAMED
Class IIIActive
4-motion® knee inlay 7411-0711
EUDAMED
Class IIIActive
A2® short stem 411305
EUDAMED
Class IIIActive
4-motion® knee tibial component 3631-R006
EUDAMED
Class IIIActive
4-motion® knee inlay 7411-1011
EUDAMED
Class IIIActive
4-motion® knee inlay 7411-0515
EUDAMED
Class IIIActive

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