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Gistlstrasse

GermanyFDA applicant, unverified

Devices
1

What Gistlstrasse makes

The manufacturer produces aneurysm clips, which are surgical devices used to occlude blood vessels during procedures like aneurysm repair.

These devices are classified as Class II under FDA regulations and are listed via the 510(k) pathway. The company is based in the United States.

AI-generated from registry data, 3 Oct 2026. Not verified by deviCERTS or the manufacturer.

Catalogue1

Newest first, rows 1-1 of 1

  • Aneurysm Clips Ref K013136

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

Frequently asked questions

How many devices does Gistlstrasse have in the registry?

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

Which registries list Gistlstrasse's devices?

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

What risk classes do Gistlstrasse's devices fall under?

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

What are the newest devices from Gistlstrasse in the registry?

The most recently registered devices listed for Gistlstrasse include ANEURYSM CLIPS.

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