KLISBio S.r.l.
ItalyFDA applicant, unverified FDA FEI 3045826185
- Devices
- 1
- Registrations
- FDA
- FDA recalls
- 0
At a glance
Market reach
- United States
- FDA FEI
What KLISBio S.r.l. makes
KLISBio S.r.l. manufactures the SILKBridge, a medical device designed for vascular applications, likely involving stent or graft delivery systems for peripheral or coronary arteries.
The SILKBridge is classified as a Class II device under FDA regulations and is listed in the FDA’s 510(k) clearance registry. The company is based in the United States.
Catalogue
SILKBridge Ref K260245
Regimes: 510(k) Registry: 510(k)
Company details
- FDA FEI number
- 3045826185
- Address
- Via L. Ariosto, 21, Bresso Milano
Frequently asked questions
How many devices does KLISBio S.r.l. have in the registry?
The registry currently lists 1 device for KLISBio S.r.l.. Devices recorded under merged duplicate company entries are counted once.
Which registries list KLISBio S.r.l.'s devices?
Among its 1 most recently registered device, KLISBio S.r.l. has devices listed in FDA 510(k) (1 device).
What risk classes do KLISBio S.r.l.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for KLISBio S.r.l.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from KLISBio S.r.l. in the registry?
The most recently registered devices listed for KLISBio S.r.l. include SILKBridge.