Covidien, LLC( Formerly Beacon Endoscopic Corp.)
United StatesFDA applicant, unverified
- Devices
- 2
What Covidien, LLC( Formerly Beacon Endoscopic Corp.) makes
Covidien, LLC manufactures fine needle aspiration and biopsy systems, including the BNX Fine Needle Aspiration System and the SHARKCORE Fine Needle Biopsy System. These devices are designed for tissue sampling in endoscopic procedures, supporting diagnostic evaluations in medical imaging.
The company’s products fall under FDA Class II regulation and are listed via 510(k) clearance. Covidien, LLC is based in the United States.
Catalogue
- Regimes: 510(k) Registry: 510(k)
Sharkcore Fine Needle Biopsy System Ref K141894
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Covidien, LLC( Formerly Beacon Endoscopic Corp.) have in the registry?
The registry currently lists 2 devices for Covidien, LLC( Formerly Beacon Endoscopic Corp.). Devices recorded under merged duplicate company entries are counted once.
Which registries list Covidien, LLC( Formerly Beacon Endoscopic Corp.)'s devices?
Among its 2 most recently registered devices, Covidien, LLC( Formerly Beacon Endoscopic Corp.) has devices listed in FDA 510(k) (2 devices).
What risk classes do Covidien, LLC( Formerly Beacon Endoscopic Corp.)'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Covidien, LLC( Formerly Beacon Endoscopic Corp.)'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Covidien, LLC( Formerly Beacon Endoscopic Corp.) in the registry?
The most recently registered devices listed for Covidien, LLC( Formerly Beacon Endoscopic Corp.) include BNX Fine Needle Aspiration System and SharkCore LG Fine Needle Biopsy System and SHARKCORE FINE NEEDLE BIOPSY SYSTEM.