Noetix, Inc.
United StatesFDA applicant, unverified
- Devices
- 3
What Noetix, Inc. makes
Noetix, Inc. makes biopsy needles, surgical extraction systems, and cystotomes used in medical procedures.
The company's devices are classified as Class I and Class II and are listed in the FDA 510(k) registry; the company is based in the United States.
Catalogue
Noetix, Biopsy Needle Ref K893992
Regimes: 510(k) Registry: 510(k)Noetix(R) Surgical Extraction(Tm) System Ref K881635
Regimes: 510(k) Registry: 510(k)Capsulectomer Cystotome Ref K871365
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Noetix, Inc. have in the registry?
The registry currently lists 3 devices for Noetix, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Noetix, Inc.'s devices?
Among its 3 most recently registered devices, Noetix, Inc. has devices listed in FDA 510(k) (3 devices).
What risk classes do Noetix, Inc.'s devices fall under?
Among its 3 most recently registered devices, the classes recorded for Noetix, Inc.'s devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from Noetix, Inc. in the registry?
The most recently registered devices listed for Noetix, Inc. include NOETIX, BIOPSY NEEDLE, NOETIX(R) SURGICAL EXTRACTION(TM) SYSTEM and CAPSULECTOMER CYSTOTOME.