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UAB "Ortho Baltic"

Lithuania LT-MF-000016954 Last updated 21 Oct 2026

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Devices
50
Registries
EUDAMED
FDA recalls
0

Catalogue50

What UAB "Ortho Baltic" makes

Ortho Baltic manufactures ankle-foot orthoses (AFOs) under the Easy Walk® brand, including models designed for stability, fixation, and mobility support. These devices are tailored to specific foot sizes and conditions, such as small, large, or extra-large sizing, and include variations like Eco and Advance II series for different clinical needs.

The company’s portfolio is classified under EU Medical Device Regulation (MDR) as Class I devices and is registered in the EU’s eudamed database. Ortho Baltic is based in Lithuania and adheres to EU regulatory requirements for these orthotic products.

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 UAB 'Ortho Baltic' manufacture?

UAB 'Ortho Baltic' specializes in manufacturing ankle-foot orthoses (AFOs) under the Easy Walk® brand. These devices are designed to support ankle stability, mobility, or fixation, catering to various foot sizes and clinical needs. Examples include models like the Easy Walk® Advance II AFO, Stability AFO, and Eco AFO, each tailored for specific patient requirements.

Where is UAB 'Ortho Baltic' based?

UAB 'Ortho Baltic' is based in Lithuania (LT). The company operates within the EU regulatory framework, ensuring its products comply with applicable standards for medical devices.

Which regulatory registries list UAB 'Ortho Baltic's' devices?

UAB 'Ortho Baltic's' devices are listed in the eudamed database, which is the EU’s central registry for medical devices. This registration ensures transparency and compliance with EU Medical Device Regulation (MDR) requirements.

How are UAB 'Ortho Baltic's' devices classified under EU regulations?

All of UAB 'Ortho Baltic's' ankle-foot orthoses (AFOs) fall under Class I classification according to the EU Medical Device Regulation (MDR). This classification applies to low-risk devices like orthotics, which typically require less stringent regulatory oversight than higher-risk categories.

AI-generated from registry data and not verified by a human reviewer.

Information

Country
Lithuania
Address
131A, Taikos pr., Kaunas, Lithuania
Phone
+370 37 473970
PRRC contact
Lina Januševičienė
EUDAMED SRN
LT-MF-000016954