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The Langer Group

Country not established

Devices
2

What The Langer Group makes

The Langer Group manufactures a counter-rotation system designed for medical applications, as well as an electrodynamogram system for diagnostic or monitoring purposes.

These devices are classified as Class I under FDA regulations and are recorded in the 510(k) clearance database. The company is based in the United States.

AI-generated from registry data, 2 Oct 2026. Not verified by deviCERTS or the manufacturer.

Catalogue2

Newest first, rows 1-2 of 2

  • Counter-Rotation System Ref K821256

    Active Regimes: 510(k) Registry: 510(k) Class:I
  • Electrodynogram System Ref K821255

    Active Regimes: 510(k) Registry: 510(k) Class:I

Frequently asked questions

How many devices does The Langer Group have in the registry?

The registry currently lists 2 devices for The Langer Group. Devices recorded under merged duplicate company entries are counted once.

Which registries list The Langer Group's devices?

Among its 2 most recently registered devices, The Langer Group has devices listed in FDA 510(k) (2 devices).

What risk classes do The Langer Group's devices fall under?

Among its 2 most recently registered devices, the classes recorded for The Langer Group's devices are Class I. Each device page shows its own class and authorisation.

What are the newest devices from The Langer Group in the registry?

The most recently registered devices listed for The Langer Group include COUNTER-ROTATION SYSTEM and ELECTRODYNOGRAM SYSTEM.

Generated automatically from registry data and not verified by a human reviewer.