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Aces GmbH

GermanyFDA applicant, unverified

Devices
1

What Aces GmbH makes

Aces GmbH makes medical devices such as the FXA, which is a type of medical device. The company's products fall under specific device categories. These devices are used in medical settings.

The portfolio of Aces GmbH is regulated and listed in the fda_510k registry, with devices classified as Class II. The company is based in the US. Its devices are subject to regulatory oversight.

AI-generated from registry data, 19 Sep 2026. Not verified by deviCERTS or the manufacturer.

Catalogue1

Newest first, rows 1-1 of 1

  • Fxa (Tm) Ref K110765

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

Frequently asked questions

How many devices does Aces GmbH have in the registry?

The registry currently lists 1 device for Aces GmbH. Devices recorded under merged duplicate company entries are counted once.

Which registries list Aces GmbH's devices?

Among its 1 most recently registered device, Aces GmbH has devices listed in FDA 510(k) (1 device).

What risk classes do Aces GmbH's devices fall under?

Among its 1 most recently registered device, the classes recorded for Aces GmbH's devices are Class II. Each device page shows its own class and authorisation.

What are the newest devices from Aces GmbH in the registry?

The most recently registered devices listed for Aces GmbH include FXA (TM).

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