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Aat Alber Antriebstechnik GmbH

US Last updated 31 May 2026

Devices
4
Registries
EUDAMEDGUDIDFDA 510(k)FDA
FDA recalls
0

Catalogue4

FDA establishments1

Registered with the FDA under this company group, matched by name.

  • AAT Alber Antriebstechnik GmbH Albstadt Baden-Wurttemberg · DE FEI 3008791629

What Aat Alber Antriebstechnik GmbH makes

Aat Alber Antriebstechnik GmbH manufactures stairclimbers, including models such as the s-max and C-MAX series (with variants like C-MAX U1, U2, and aviation-specific S-MAX). They also produce powered wheelchairs under the S-MAX and C-MAX brands, designed for mobility assistance in various settings.

Their devices fall under FDA Class II regulation and are recorded in the FDA’s 510(k) and UDI registries. The company is based in 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 Aat Alber Antriebstechnik GmbH primarily manufacture?

Aat Alber Antriebstechnik GmbH specializes in mobility assistance devices, focusing on stairclimbers like the s-max and C-MAX series (including variants such as C-MAX U1, U2, and aviation-specific models like S-MAX AVIATION). They also produce powered wheelchairs under the S-MAX and C-MAX brands, catering to users needing enhanced mobility in different environments.

Where is Aat Alber Antriebstechnik GmbH based?

The company is headquartered in the United States, where it develops and manufactures its mobility devices, including stairclimbers and powered wheelchairs.

Which regulatory registries list Aat Alber Antriebstechnik GmbH’s devices?

The company’s devices are recorded in the FDA’s 510(k) premarket notification program and the FDA’s Unique Device Identifier (UDI) system. These registries track devices classified under FDA regulations.

How are Aat Alber Antriebstechnik GmbH’s devices classified by regulatory authorities?

The company’s stairclimbers and powered wheelchairs fall under FDA Class II classification. This classification applies to devices deemed to have an acceptable level of risk when properly used, requiring special controls beyond general controls to ensure safety and effectiveness.

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

Information

Country
US
DUNS number
314612359