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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 2 of 5
DeviceModel / ReferenceRegistriesClassStatus
A2® Eröffnungsraspel 9110100
EUDAMED
Class IActive
4-motion® Probeinlay C h=12 9211312
EUDAMED
Class IIaActive
4-motion® Probefemur rechts 7w 9210808
EUDAMED
Class IIaActive
4-motion® Probeinlay B h=12 9211212
EUDAMED
Class IIaActive
BSM Heber, Rechts, Groß 9211610-08
EUDAMED
Class IActive
Siebeinsatz für MP Köpfe 9111100
EUDAMED
Class IActive
4-motion® Drehmomentschlüssel 9211601
EUDAMED
Class IActive
4-motion® Winkelbuchse 3° 9211523
EUDAMED
Class IActive
4-motion® Probefemur links 6s 9210705
EUDAMED
Class IIaActive
4-motion® Kielmeißel Tibia PSA Gr. 1-3 9211412
EUDAMED
Class IActive
4-motion® Universeller Handgriff 9211500
EUDAMED
Class IActive
4-motion® Tibia-Größenlehre Gr.6 9210906
EUDAMED
Class IIaActive
4-motion® Probeinlay B h=6 9211206
EUDAMED
Class IIaActive
4-motion® Aufsatz Femurausschläger 9211503
EUDAMED
Class IActive
4-motion® Tibia Ausrichtlehre EX-TAL 9211001
EUDAMED
Class IActive
BSM Aufsatz Extension 9211610-10
EUDAMED
Class IActive
4-motion® Tibiagrößenlehre PSA Gr. 7 9210917
EUDAMED
Class IIaActive
4-motion® Tibiagrößenlehre PSA Gr. 2 9210912
EUDAMED
Class IIaActive
Schaft-Sieb 9110000
EUDAMED
Class IActive
4-motion® Probeinlay A h=10 9211110
EUDAMED
Class IIaActive
4-motion® Tibiagrößenlehre PSA Gr. 9 9210919
EUDAMED
Class IIaActive
4-motion® Kielmeißel Tibia PSA Gr. 7-10 9211414
EUDAMED
Class IActive
4-motion® Probefemur links 8w 9210709
EUDAMED
Class IIaActive
4-motion® Kielmeißel Gr. 7-10 9211403
EUDAMED
Class IActive
4-motion® Tibia-Größenlehre Gr. 1 9210901
EUDAMED
Class IIaActive
4-motion® 4in1 Schnittblock Gr. 3 9210603
EUDAMED
Class IActive
4-motion® Kielmeißel Tibia PSA Gr. 4-6 9211413
EUDAMED
Class IActive
4-motion® Winkelbuchse 2° 9211522
EUDAMED
Class IActive
4-motion® 4in1 Schnittblock Gr. 7 9210607
EUDAMED
Class IActive
4-motion® Probefemur links 6w 9210707
EUDAMED
Class IIaActive
4-motion® Probefemur links 5s 9210704
EUDAMED
Class IIaActive
4-motion® Tibia-Größenlehre Gr.4 9210904
EUDAMED
Class IIaActive
4-motion® Probeinlay A h=8 9211108
EUDAMED
Class IIaActive
BSM Heber, Links, Std. 9211610-05
EUDAMED
Class IActive
4-motion® Instrumenten-Sieb Deckel 9110001
EUDAMED
Class IActive
4-motion® Tibiagrößenlehre PSA Gr. 1 9210911
EUDAMED
Class IIaActive
4-motion® Kielmeißel Gr. 4-6 9211402
EUDAMED
Class IActive
4-motion® Tibiagrößenlehre PSA Gr. 6 9210916
EUDAMED
Class IIaActive
4-motion® Tibia-Größenlehre Gr. 9 9210909
EUDAMED
Class IIaActive
4-motion® Probeinlay B h=8 9211208
EUDAMED
Class IIaActive
4-motion® Drillpin 3, 2 mit Kopf 9210202
EUDAMED
Class IIaActive
4-motion® Probefemur links 5w 9210706
EUDAMED
Class IIaActive
4-motion® Drillpin 3, 2 9210201
EUDAMED
Class IIaActive
4-motion® Probefemur links 2s 9210701
EUDAMED
Class IIaActive
4-motion® Pinzange 9210300
EUDAMED
Class IActive
4-motion® Tibiabohrer 9210502
EUDAMED
Class IIaActive
4-motion® Probefemur links 4s 9210703
EUDAMED
Class IIaActive
4-motion® Trochleafeile 9211410
EUDAMED
Class IActive
4-motion® Tibiagrößenlehre PSA Gr. 5 9210915
EUDAMED
Class IIaActive
4-motion® Verlängerung für Ausrichtstab 9211512
EUDAMED
Class IActive

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