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Beacon Surgical, Inc.

United StatesFDA applicant, unverified

Devices
2

Catalogue2

Newest first, rows 1-2 of 2

  • Retrieval bag system Ref K151489

    Active Regimes: 510(k) Registry: 510(k) Class:II
  • Pelican Sling Retractor Ref K153542

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

Frequently asked questions

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

The registry currently lists 2 devices for Beacon Surgical, Inc.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Beacon Surgical, Inc.'s devices?

Among its 2 most recently registered devices, Beacon Surgical, Inc. has devices listed in FDA 510(k) (2 devices).

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

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

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

The most recently registered devices listed for Beacon Surgical, Inc. include Retrieval bag system and Pelican Sling Retractor.

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