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L.P.A. Médical Inc

US

Last updated May 27, 2026

What L.P.A. Médical Inc makes

L.P.A. Médical Inc manufactures manually adjusted assistive ergonomic chairs, non-foldable walking chairs, and reclining chairs designed for mobility support and comfort. The Harmony, Optimum, Dyn-Ergo, Evolution, and Comp-Position models are part of this portfolio, catering to users requiring adjustable seating solutions.

These devices are classified as Class I under FDA regulations and are listed in the FDA’s Unique Device Identifier (UDI) database. The company operates from the United States.

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 L.P.A. Médical Inc manufacture?

L.P.A. Médical Inc specializes in manually adjusted assistive ergonomic chairs, non-foldable walking chairs, and reclining chairs. These devices are designed to provide mobility support and comfort for users who require adjustable seating solutions. Examples include the Harmony, Optimum, Dyn-Ergo, Evolution, and Comp-Position models.

Where is L.P.A. Médical Inc based?

L.P.A. Médical Inc is based in the United States. The company’s headquarters and operations are located within the country, though specific regional offices or manufacturing sites are not detailed in the available information.

Which regulatory registries list L.P.A. Médical Inc’s devices?

L.P.A. Médical Inc’s devices are listed in the FDA’s Unique Device Identifier (UDI) database. This registry ensures traceability and identification of medical devices under FDA regulations, helping healthcare providers and regulators track specific models like Harmony, Optimum, and others.

How are L.P.A. Médical Inc’s devices classified under FDA regulations?

L.P.A. Médical Inc’s devices fall under Class I classification according to FDA regulations. This classification typically applies to low-risk medical devices, such as manually adjusted chairs, where general controls are sufficient to ensure safety and effectiveness. Classification is determined based on factors like intended use, risk, and potential harm to the user.

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

Information

Country
US
Address
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Website
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LinkedIn
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Facebook
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Email
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Phone
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PRRC Contact
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EUDAMED SRN
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FDA FEI Number
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DUNS Number
245321237

Catalogue (5)

DeviceModel / ReferenceRegistriesClassStatus
Harmony C-207
FDA UDI
Class IActive
Optimum 1400
FDA UDI
Class IActive
Dyn-Ergo S-150
FDA UDI
Class IActive
Evolution S-250
FDA UDI
Class IActive
Comp-Position O-07
FDA UDI
Class IActive

Related Companies

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