Beacon Endoscopic
Country not established
- Devices
- 1
What Beacon Endoscopic makes
Beacon Endoscopic manufactures endoscopic needle delivery systems, including pre-loaded and individually sterile-packed needles in 19, 22, and 25 gauge sizes for medical procedures.
These devices are classified as Class II under FDA regulations and are listed via the 510(k) pathway. The company is based in the United States.
Catalogue
- Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Beacon Endoscopic have in the registry?
The registry currently lists 1 device for Beacon Endoscopic. Devices recorded under merged duplicate company entries are counted once.
Which registries list Beacon Endoscopic's devices?
Among its 1 most recently registered device, Beacon Endoscopic has devices listed in FDA 510(k) (1 device).
What risk classes do Beacon Endoscopic's devices fall under?
Among its 1 most recently registered device, the classes recorded for Beacon Endoscopic's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Beacon Endoscopic in the registry?
The most recently registered devices listed for Beacon Endoscopic include BNX DELIVERY SYSTEM PRE-LOADED WITH 19, 22 AND 25 GAUGE NEEDLE, 19, 22 OR 25 GAUGE NEEDLES (INDIVIDUALLY STERILE-PACKED,.