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PROTETIKA, 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
LinkedIn
—
Phone
+421903433065
PRRC Contact
Katarína Keimová
EUDAMED SRN
SK-MF-000004489
FDA FEI Number
—
DUNS Number
—

Catalogue (415)

Page 9 of 9
DeviceModel / ReferenceRegistriesClassStatus
Bandáž napomínacia, guma, typ I J 39793
EUDAMED
Class IActive
Neoprénová bandáž zápästia ZA-4, PRAVÁ J 22121
EUDAMED
Class IActive
Pás lumbosakrály s dlahami a gumovým ťahom, Sohatex J 77984
EUDAMED
Class IActive
Ortéza zápästia, laminovaný materiál, ĽAVÁ, ZA-51 J 94658
EUDAMED
Class IActive
Neoprénová bandáž kolena KO-3 J 22129
EUDAMED
Class IActive
Neoprénová bandáž lakťa LA-4 J 22126
EUDAMED
Class IActive
Gumotextilná ortéza kolena KO-21 J 69587
EUDAMED
Class IActive
Neoprénová bandáž drieku J 22117
EUDAMED
Class IActive
Neoprénová bandáž drieku PA-1 J 22116
EUDAMED
Class IActive
Neoprénová bandáž drieku J 22117
EUDAMED
Class IActive
Neoprénová bandáž zápästia ZA-3 J 22120
EUDAMED
Class IActive
Neoprenová bandáž kolena KO-6 J 58378
EUDAMED
Class IActive
Korzet gumotextilný J 52711
EUDAMED
Class IActive
Neoprénová ortéza kolena KO-12 J 53692
EUDAMED
Class IActive
Ortéza zápästia, laminovaný materiál, ĽAVÁ, ZA-52 J 94659
EUDAMED
Class IActive
Pás lumbosakrálny s dlahami a gumovým ťahom, Sohatex J 77984
EUDAMED
Class IActive

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