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Gyrx, LLC

United StatesFDA applicant, unverified

Devices
2

What Gyrx, LLC makes

Gyrx, LLC manufactures surgical clip appliers, including the TI Clip Applier and the Visu-Lock 5mm Clip Applier, designed for tissue approximation and ligation in minimally invasive procedures.

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, 1 Oct 2026. Not verified by deviCERTS or the manufacturer.

Catalogue2

Newest first, rows 1-2 of 2

  • Ti Clip Applier Ref K034029

    Active Regimes: 510(k) Registry: 510(k) Class:II
  • Visu-Lock 5mm Clip Applier Ref K033161

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

Frequently asked questions

How many devices does Gyrx, LLC have in the registry?

The registry currently lists 2 devices for Gyrx, LLC. Devices recorded under merged duplicate company entries are counted once.

Which registries list Gyrx, LLC's devices?

Among its 2 most recently registered devices, Gyrx, LLC has devices listed in FDA 510(k) (2 devices).

What risk classes do Gyrx, LLC's devices fall under?

Among its 2 most recently registered devices, the classes recorded for Gyrx, LLC's devices are Class II. Each device page shows its own class and authorisation.

What are the newest devices from Gyrx, LLC in the registry?

The most recently registered devices listed for Gyrx, LLC include TI CLIP APPLIER and VISU-LOCK 5MM CLIP APPLIER.

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