Lixi, Inc.
United StatesFDA applicant, unverified
- Devices
- 2
What Lixi, Inc. makes
Lixi, Inc. manufactures imaging scopes, including the Lixiscope (also branded as LIXI) and its modified variants, designed for diagnostic and procedural visualization in medical settings.
These devices are classified as Class II under FDA regulations and are authorised via the 510(k) clearance process. The company is based in the United States.
Catalogue
Lixiscope - Or Lixi Ref K820658
Regimes: 510(k) Registry: 510(k)Lixi Imaging Scope. Modification Ref K925251
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Lixi, Inc. have in the registry?
The registry currently lists 2 devices for Lixi, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Lixi, Inc.'s devices?
Among its 2 most recently registered devices, Lixi, Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do Lixi, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Lixi, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Lixi, Inc. in the registry?
The most recently registered devices listed for Lixi, Inc. include LIXISCOPE - OR LIXI and LIXI IMAGING SCOPE. MODIFICATION.