N-Tech Endoscopy, Inc.
United StatesFDA 510(k) applicant, unverified
- Devices
- 3
What N-Tech Endoscopy, Inc. makes
N-Tech Endoscopy, Inc. manufactures endoscopic devices including laparoscopes, arthroscopes, and cystoscopes.
The company's devices are Class II and listed in the FDA 510(k) registry. N-Tech Endoscopy, Inc. is based in the US.
Catalogue
- 510(k) 510(k)
Ntech Arthroscope Ref K980599
510(k) 510(k)Ntech Cystoscopes Ref K980592
510(k) 510(k)
Frequently asked questions
How many devices does N-Tech Endoscopy, Inc. have in the registry?
The registry currently lists 3 devices for N-Tech Endoscopy, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list N-Tech Endoscopy, Inc.'s devices?
Among its 3 most recently registered devices, N-Tech Endoscopy, Inc. has devices listed in FDA 510(k) (3 devices).
What risk classes do N-Tech Endoscopy, Inc.'s devices fall under?
Among its 3 most recently registered devices, the classes recorded for N-Tech Endoscopy, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from N-Tech Endoscopy, Inc. in the registry?
The most recently registered devices listed for N-Tech Endoscopy, Inc. include N TECH DOUBLE PUNCTURE LAPAROSCOPE/N TECH OPERATING LAPAROSCOPE, NTECH ARTHROSCOPE and NTECH CYSTOSCOPES.