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Enovis

Country not established

Devices
1

What Enovis makes

Enovis manufactures the ManaFuse, a vascular closure device designed to seal arterial puncture sites after procedures such as coronary angiography or percutaneous coronary intervention. This product is intended to reduce bleeding risks and promote faster patient recovery by ensuring effective hemostasis at the access site.

The company’s portfolio is regulated under the FDA’s Premarket Approval (PMA) pathway, reflecting its classification as a high-risk medical device. The ManaFuse is listed in the FDA’s PMA registry, and the manufacturer operates from the United States.

AI-generated from registry data, 20 Sep 2026. Not verified by deviCERTS or the manufacturer.

Catalogue1

Newest first, rows 1-1 of 1

  • ManaFuse Ref P210016

    Active Regimes: PMA Registry: PMA Class:—

Frequently asked questions

How many devices does Enovis have in the registry?

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

Which registries list Enovis's devices?

Among its 1 most recently registered device, Enovis has devices listed in FDA PMA (1 device).

What are the newest devices from Enovis in the registry?

The most recently registered devices listed for Enovis include ManaFuse.

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