Scitex Corporation, Ltd.
IsraelFDA applicant, unverified
- Devices
- 1
What Scitex Corporation, Ltd. makes
Scitex Corporation, Ltd. manufactures the UNITONE, a medical device designed for single-use, disposable applications in surgical procedures.
The UNITONE is classified as a Class II device under FDA regulations and is listed via the 510(k) pathway. The company is based in the United States.
Catalogue
Unitone Ref K934572
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Scitex Corporation, Ltd. have in the registry?
The registry currently lists 1 device for Scitex Corporation, Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Scitex Corporation, Ltd.'s devices?
Among its 1 most recently registered device, Scitex Corporation, Ltd. has devices listed in FDA 510(k) (1 device).
What risk classes do Scitex Corporation, Ltd.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Scitex Corporation, Ltd.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Scitex Corporation, Ltd. in the registry?
The most recently registered devices listed for Scitex Corporation, Ltd. include UNITONE.