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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 1 of 5
DeviceModel / ReferenceRegistriesClassStatus
4-motion® Probefemur rechts 4s 9210803
EUDAMED
Class IIaActive
4-motion® 4in1 Schnittblock Gr. 5 9210605
EUDAMED
Class IActive
4-motion® Distaler Femur-Justierblock DFJ 9211704
EUDAMED
Class IActive
4-motion® Probeinlay C h=8 9211308
EUDAMED
Class IIaActive
4-motion® Probefemur links 7w 9210708
EUDAMED
Class IIaActive
4-motion® Probeinlay A h=6 9211106
EUDAMED
Class IIaActive
4-motion® Probefemur links 9w 9210710
EUDAMED
Class IIaActive
4-motion® Winkelbuchse 1° 9211521
EUDAMED
Class IActive
4-motion® Tibia-Justierblock links 9211702
EUDAMED
Class IActive
4-motion® Kortikalisfühler 1, 27 mm 9210401
EUDAMED
Class IActive
4-motion® Probefemur rechts 8w 9210809
EUDAMED
Class IIaActive
4-motion® Tibia-Größenlehre Gr. 10 9210910
EUDAMED
Class IIaActive
4-motion® Probeinlay C h=10 9211310
EUDAMED
Class IIaActive
4-motion® Aufsatz Femur-/Tibiaeinschläger 9211501
EUDAMED
Class IActive
4-motion® Femurbohrer 6, 4 9210501
EUDAMED
Class IIaActive
4-motion® Probefemur rechts 2s 9210801
EUDAMED
Class IIaActive
4-motion® Ausrichtstab 9211511
EUDAMED
Class IActive
4-motion® Korrekturblock Tibia 9211701
EUDAMED
Class IActive
4-motion® Tibiagrößenlehre PSA Gr. 8 9210918
EUDAMED
Class IIaActive
4-motion® Tibiabohrer PSA 9210503
EUDAMED
Class IIaActive
4-motion® Probefemur rechts 3s 9210802
EUDAMED
Class IIaActive
4-motion® Tibia-Größenlehre Gr.5 9210905
EUDAMED
Class IIaActive
4-motion® Aufsatz Inlayeinschläger 9211502
EUDAMED
Class IActive
4-motion® 4in1 Schnittblock Gr. 8 9210608
EUDAMED
Class IActive
4-motion® Tibiagrößenlehre PSA Gr. 3 9210913
EUDAMED
Class IIaActive
4-motion® Korrekturblock Femur 9211700
EUDAMED
Class IActive
4-motion® Bohr- und Meißelführung 9211400
EUDAMED
Class IActive
4-motion® Probeinlay C h=6 9211306
EUDAMED
Class IIaActive
4-motion® Bohr- und Meißelführung PSA 9211411
EUDAMED
Class IActive
Manipulierhals Raspel 9110601
EUDAMED
Class IIaActive
4-motion® Probeinlay B h=10 9211210
EUDAMED
Class IIaActive
BSM Heber, Links, Groß 9211610-07
EUDAMED
Class IActive
BSM Tibia Auflageplatte, Std. 9211610-02
EUDAMED
Class IActive
BSM Aufsatz Flexion 9211610-09
EUDAMED
Class IActive
DO Raspel-Adapter 50/15 links mit Schlagplatte 9110401
EUDAMED
Class IActive
4-motion® Probefemur links 3s 9210702
EUDAMED
Class IIaActive
4-motion® Tibia-Größenlehre Gr.8 9210908
EUDAMED
Class IIaActive
4-motion® 4in1 Schnittblock Gr. 9 9210609
EUDAMED
Class IActive
4-motion® 4in1 Schnittblock Gr. 4 9210604
EUDAMED
Class IActive
A2® Schaftraspel 0 G 9110200
EUDAMED
Class IIaActive
4-motion® Tibia-Justierblock rechts 9211703
EUDAMED
Class IActive
4-motion® Probefemur rechts 5w 9210806
EUDAMED
Class IIaActive
BSM Grundteil 9211610-01
EUDAMED
Class IActive
BSM Heber, Rechts Std. 9211610-06
EUDAMED
Class IActive
BSM Tibia Auflageplatte, Groß 9211610-03
EUDAMED
Class IActive
4-motion® Instrumenten-Sieb 9210000
EUDAMED
Class IActive
4-motion® Probefemur rechts 6s 9210805
EUDAMED
Class IIaActive
4-motion® Tibiagrößenlehre PSA Gr. 4 9210914
EUDAMED
Class IIaActive
4-motion® Femurbohrer Ø8 9210504
EUDAMED
Class IIaActive
4-motion® Probefemur rechts 9w 9210810
EUDAMED
Class IIaActive

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