Sohniks Endoscopy, Inc.
United StatesFDA applicant, unverified
- Devices
- 2
What Sohniks Endoscopy, Inc. makes
Sohniks Endoscopy, Inc. manufactures endoscopic devices marketed under the name SOHNIKS.
These devices are classified as Class II medical devices and are listed in the FDA 510(k) registry; the company is based in the United States.
Catalogue
Frequently asked questions
How many devices does Sohniks Endoscopy, Inc. have in the registry?
The registry currently lists 2 devices for Sohniks Endoscopy, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Sohniks Endoscopy, Inc.'s devices?
Among its 2 most recently registered devices, Sohniks Endoscopy, Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do Sohniks Endoscopy, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Sohniks Endoscopy, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Sohniks Endoscopy, Inc. in the registry?
The most recently registered devices listed for Sohniks Endoscopy, Inc. include SOHNIKS.