Cambridge Endoscopic Devices
Country not established
- Devices
- 1
What Cambridge Endoscopic Devices makes
Cambridge Endoscopic Devices manufactures endoscopic surgical instruments, including the PUREWRIST SCISSORS (model PW1101-01), PUREWRIST DISSECTOR (model PW1201-01), and PUREWRIST HOOK (model PW1301-01). These tools are designed for minimally invasive procedures, aiding in tissue dissection, cutting, and manipulation during laparoscopic or endoscopic surgeries.
The company’s endoscopic instruments are classified as Class II devices under FDA regulations and are supported by 510(k) clearances. The portfolio is listed in the FDA’s 510(k) database, reflecting their regulatory status. The manufacturer is based in the United States.
Catalogue
Purewrist Scissors, Model PW1101-01;PUREWRIST Dissector, Model PW1201-01;PUREWRIST Hook, Model PW1301-01 Ref K061425
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Cambridge Endoscopic Devices have in the registry?
The registry currently lists 1 device for Cambridge Endoscopic Devices. Devices recorded under merged duplicate company entries are counted once.
Which registries list Cambridge Endoscopic Devices's devices?
Among its 1 most recently registered device, Cambridge Endoscopic Devices has devices listed in FDA 510(k) (1 device).
What risk classes do Cambridge Endoscopic Devices's devices fall under?
Among its 1 most recently registered device, the classes recorded for Cambridge Endoscopic Devices's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Cambridge Endoscopic Devices in the registry?
The most recently registered devices listed for Cambridge Endoscopic Devices include PUREWRIST SCISSORS, MODEL PW1101-01;PUREWRIST DISSECTOR, MODEL PW1201-01;PUREWRIST HOOK, MODEL PW1301-01.