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Hoechst-Roussel Pharmaceuticals, Inc.

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Devices
1

What Hoechst-Roussel Pharmaceuticals, Inc. makes

The company produces the RAP/TEX-LGM Kit, a medical device designed for surgical applications involving tissue reinforcement or fixation, likely intended for soft tissue or vascular procedures.

This product is classified as Class II under FDA regulations and is listed via 510(k) clearance. The manufacturer is based in the United States.

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

Catalogue1

Newest first, rows 1-1 of 1

  • Rapi/Tex-Lgm Kit Ref K760673

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

Frequently asked questions

How many devices does Hoechst-Roussel Pharmaceuticals, Inc. have in the registry?

The registry currently lists 1 device for Hoechst-Roussel Pharmaceuticals, Inc.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Hoechst-Roussel Pharmaceuticals, Inc.'s devices?

Among its 1 most recently registered device, Hoechst-Roussel Pharmaceuticals, Inc. has devices listed in FDA 510(k) (1 device).

What risk classes do Hoechst-Roussel Pharmaceuticals, Inc.'s devices fall under?

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

What are the newest devices from Hoechst-Roussel Pharmaceuticals, Inc. in the registry?

The most recently registered devices listed for Hoechst-Roussel Pharmaceuticals, Inc. include RAPI/TEX-LGM KIT.

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