Canada Endoscope Corporation
CanadaFDA applicant, unverified
- Devices
- 1
What Canada Endoscope Corporation makes
Canada Endoscope Corporation manufactures rigid cystoscopes, including models such as the CE0004-C, CE006-C, CE3004-C, CE3027-C, CE7004-C, CE1204-C, and CE1227-C. These devices are designed for diagnostic and therapeutic procedures within the urinary bladder and lower urinary tract, enabling visualization of internal structures.
The company’s cystoscope portfolio is classified as Class II under FDA regulations and is listed via the 510(k) clearance process. These devices are intended for use in the United States, where they are subject to compliance with the FDA’s medical device authorization requirements.
Catalogue
- Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Canada Endoscope Corporation have in the registry?
The registry currently lists 1 device for Canada Endoscope Corporation. Devices recorded under merged duplicate company entries are counted once.
Which registries list Canada Endoscope Corporation's devices?
Among its 1 most recently registered device, Canada Endoscope Corporation has devices listed in FDA 510(k) (1 device).
What risk classes do Canada Endoscope Corporation's devices fall under?
Among its 1 most recently registered device, the classes recorded for Canada Endoscope Corporation's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Canada Endoscope Corporation in the registry?
The most recently registered devices listed for Canada Endoscope Corporation include CYSTOSCOPE, MODELS CE0004-C, CE006-C, CE3004-C, CE3027-C, CE7004-C, CE1204-C, CE1227-C.