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Bioeconeer, Inc.

TaiwanFDA applicant, unverified

Devices
1

What Bioeconeer, Inc. makes

Bioeconeer, Inc. manufactures the ACE Monopolar Attachment, a device designed for use in surgical electrocautery procedures to enhance precision and control during tissue dissection or coagulation.

The ACE Monopolar Attachment is classified as a Class II medical device under FDA regulations and is 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

  • Ace Monopolar Attachment Ref K123061

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

Frequently asked questions

How many devices does Bioeconeer, Inc. have in the registry?

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

Which registries list Bioeconeer, Inc.'s devices?

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

What risk classes do Bioeconeer, Inc.'s devices fall under?

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

What are the newest devices from Bioeconeer, Inc. in the registry?

The most recently registered devices listed for Bioeconeer, Inc. include ACE MONOPOLAR ATTACHMENT.

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