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Sign in to claim this brandPROTETIKA, a.s.
Slovakia·SK-MF-000004489
Last updated September 17, 2026
About
Welcome to the website of the leading manufacturer of medical shoes and medical devices.
Translated from the manufacturer's own website. Source
What PROTETIKA, a.s. makes
The company manufactures orthopedic foot insoles for adults, children, and gender-specific designs to address flat feet (both longitudinal and transverse), as well as neoprene hip bandages for support. It also produces knee orthoses with silicone pads, knee immobilizers with movement restrictions, and wrist orthoses without straps, alongside abdominal health belts classified as medical devices.
All listed devices fall under Class I medical device regulations and are registered in the EUDAMED database. The manufacturer is based in Slovakia.
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 Protetika, a.s. manufacture?
Protetika, a.s. specializes in Class I medical devices primarily focused on orthopedic support. Their product range includes custom orthopedic foot insoles designed for adults, children, and gender-specific use to address flat feet (both longitudinal and transverse). They also produce neoprene hip bandages for support, knee orthoses with silicone pads, knee immobilizers that restrict movement, and wrist orthoses without straps. Additionally, they manufacture abdominal health belts classified as medical devices.
Where is Protetika, a.s. based?
Protetika, a.s. is based in Slovakia, as indicated by its country designation. The company’s manufacturing and operations are centered there, serving markets where its Class I orthopedic and support devices are utilized.
Which regulatory registries list Protetika, a.s.’s devices?
Protetika, a.s.’s devices are registered in the EUDAMED database, which is the European Union’s medical device registry. This platform is used to track and provide transparency on authorized medical devices within the EU, ensuring compliance with regulatory requirements.
How are Protetika, a.s.’s devices classified under medical device regulations?
All of Protetika, a.s.’s devices fall under Class I medical device regulations. This classification applies to low-risk devices, such as orthopedic insoles, bandages, and certain orthoses, which typically require less stringent regulatory oversight compared to higher-risk categories.
AI-generated from registry data and not verified by a human reviewer.
Information
- Country
- Slovakia
- Address
- 10, Bojnická, Bratislava, Slovakia
- Website
- www.protetika.sk
- —
- sk-sk.facebook.com/ProtetikaObuv
- [email protected]
- Phone
- +421903433065
- PRRC Contact
- Katarína Keimová
- EUDAMED SRN
- SK-MF-000004489
- FDA FEI Number
- —
- DUNS Number
- —
Catalogue (416)
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