Scilex, Ltd.
IsraelFDA applicant, unverified
- Devices
- 1
What Scilex, Ltd. makes
Scilex, Ltd. manufactures the PETERIO Universal Laser Scanning Handpiece, a device designed for precise laser-assisted surgical procedures in ophthalmology, particularly for corneal and anterior segment applications.
The company’s portfolio is regulated under FDA Class II devices and requires 510(k) clearance for market authorisation. The handpiece is listed in the FDA’s 510(k) registry. Scilex, Ltd. is based in the United States.
Catalogue
Peterio Universal Laser Scanning Handpiece Ref K073048
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Scilex, Ltd. have in the registry?
The registry currently lists 1 device for Scilex, Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Scilex, Ltd.'s devices?
Among its 1 most recently registered device, Scilex, Ltd. has devices listed in FDA 510(k) (1 device).
What risk classes do Scilex, Ltd.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Scilex, Ltd.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Scilex, Ltd. in the registry?
The most recently registered devices listed for Scilex, Ltd. include PETERIO UNIVERSAL LASER SCANNING HANDPIECE.