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Sign in to claim this brandARTIQO 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
- —
- —
- [email protected]
- Phone
- +49 2591-8931500
- PRRC Contact
- Mario Frank
- EUDAMED SRN
- DE-MF-000007336
- FDA FEI Number
- —
- DUNS Number
- —
Catalogue (238)
Page 1 of 5| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| 4-motion® Probefemur rechts 4s | 9210803 | EUDAMED | Class IIa | Active |
| 4-motion® 4in1 Schnittblock Gr. 5 | 9210605 | EUDAMED | Class I | Active |
| 4-motion® Distaler Femur-Justierblock DFJ | 9211704 | EUDAMED | Class I | Active |
| 4-motion® Probeinlay C h=8 | 9211308 | EUDAMED | Class IIa | Active |
| 4-motion® Probefemur links 7w | 9210708 | EUDAMED | Class IIa | Active |
| 4-motion® Probeinlay A h=6 | 9211106 | EUDAMED | Class IIa | Active |
| 4-motion® Probefemur links 9w | 9210710 | EUDAMED | Class IIa | Active |
| 4-motion® Winkelbuchse 1° | 9211521 | EUDAMED | Class I | Active |
| 4-motion® Tibia-Justierblock links | 9211702 | EUDAMED | Class I | Active |
| 4-motion® Kortikalisfühler 1, 27 mm | 9210401 | EUDAMED | Class I | Active |
| 4-motion® Probefemur rechts 8w | 9210809 | EUDAMED | Class IIa | Active |
| 4-motion® Tibia-Größenlehre Gr. 10 | 9210910 | EUDAMED | Class IIa | Active |
| 4-motion® Probeinlay C h=10 | 9211310 | EUDAMED | Class IIa | Active |
| 4-motion® Aufsatz Femur-/Tibiaeinschläger | 9211501 | EUDAMED | Class I | Active |
| 4-motion® Femurbohrer 6, 4 | 9210501 | EUDAMED | Class IIa | Active |
| 4-motion® Probefemur rechts 2s | 9210801 | EUDAMED | Class IIa | Active |
| 4-motion® Ausrichtstab | 9211511 | EUDAMED | Class I | Active |
| 4-motion® Korrekturblock Tibia | 9211701 | EUDAMED | Class I | Active |
| 4-motion® Tibiagrößenlehre PSA Gr. 8 | 9210918 | EUDAMED | Class IIa | Active |
| 4-motion® Tibiabohrer PSA | 9210503 | EUDAMED | Class IIa | Active |
| 4-motion® Probefemur rechts 3s | 9210802 | EUDAMED | Class IIa | Active |
| 4-motion® Tibia-Größenlehre Gr.5 | 9210905 | EUDAMED | Class IIa | Active |
| 4-motion® Aufsatz Inlayeinschläger | 9211502 | EUDAMED | Class I | Active |
| 4-motion® 4in1 Schnittblock Gr. 8 | 9210608 | EUDAMED | Class I | Active |
| 4-motion® Tibiagrößenlehre PSA Gr. 3 | 9210913 | EUDAMED | Class IIa | Active |
| 4-motion® Korrekturblock Femur | 9211700 | EUDAMED | Class I | Active |
| 4-motion® Bohr- und Meißelführung | 9211400 | EUDAMED | Class I | Active |
| 4-motion® Probeinlay C h=6 | 9211306 | EUDAMED | Class IIa | Active |
| 4-motion® Bohr- und Meißelführung PSA | 9211411 | EUDAMED | Class I | Active |
| Manipulierhals Raspel | 9110601 | EUDAMED | Class IIa | Active |
| 4-motion® Probeinlay B h=10 | 9211210 | EUDAMED | Class IIa | Active |
| BSM Heber, Links, Groß | 9211610-07 | EUDAMED | Class I | Active |
| BSM Tibia Auflageplatte, Std. | 9211610-02 | EUDAMED | Class I | Active |
| BSM Aufsatz Flexion | 9211610-09 | EUDAMED | Class I | Active |
| DO Raspel-Adapter 50/15 links mit Schlagplatte | 9110401 | EUDAMED | Class I | Active |
| 4-motion® Probefemur links 3s | 9210702 | EUDAMED | Class IIa | Active |
| 4-motion® Tibia-Größenlehre Gr.8 | 9210908 | EUDAMED | Class IIa | Active |
| 4-motion® 4in1 Schnittblock Gr. 9 | 9210609 | EUDAMED | Class I | Active |
| 4-motion® 4in1 Schnittblock Gr. 4 | 9210604 | EUDAMED | Class I | Active |
| A2® Schaftraspel 0 G | 9110200 | EUDAMED | Class IIa | Active |
| 4-motion® Tibia-Justierblock rechts | 9211703 | EUDAMED | Class I | Active |
| 4-motion® Probefemur rechts 5w | 9210806 | EUDAMED | Class IIa | Active |
| BSM Grundteil | 9211610-01 | EUDAMED | Class I | Active |
| BSM Heber, Rechts Std. | 9211610-06 | EUDAMED | Class I | Active |
| BSM Tibia Auflageplatte, Groß | 9211610-03 | EUDAMED | Class I | Active |
| 4-motion® Instrumenten-Sieb | 9210000 | EUDAMED | Class I | Active |
| 4-motion® Probefemur rechts 6s | 9210805 | EUDAMED | Class IIa | Active |
| 4-motion® Tibiagrößenlehre PSA Gr. 4 | 9210914 | EUDAMED | Class IIa | Active |
| 4-motion® Femurbohrer Ø8 | 9210504 | EUDAMED | Class IIa | Active |
| 4-motion® Probefemur rechts 9w | 9210810 | EUDAMED | Class IIa | Active |
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