Invatec S.p.A.
Country not established
- Devices
- 4
What Invatec S.p.A. makes
Invatec S.P.A. manufactures percutaneous transluminal angioplasty (PTA) balloon dilatation catheters, including low-profile and high-pressure variants for vascular interventions. Their portfolio also includes biliary stent systems for treating bile duct obstructions and a proximal cerebral protection device designed to reduce embolic risk during neurovascular procedures.
The company’s devices are classified as Class II under FDA regulations and are authorised via the 510(k) pathway. These products are listed in the FDA’s 510(k) registry. The manufacturer is based in the United States.
Catalogue
- Regimes: 510(k) Registry: 510(k)
Admiral Xtreme Pta Balloon Dilatation Catheter Ref K100921
Regimes: 510(k) Registry: 510(k)Scuba Biliary Stent System Ref K092352
Regimes: 510(k) Registry: 510(k)- Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Invatec S.P.A. have in the registry?
The registry currently lists 4 devices for Invatec S.P.A.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Invatec S.P.A.'s devices?
Among its 4 most recently registered devices, Invatec S.P.A. has devices listed in FDA 510(k) (4 devices).
What risk classes do Invatec S.P.A.'s devices fall under?
Among its 4 most recently registered devices, the classes recorded for Invatec S.P.A.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Invatec S.P.A. in the registry?
The most recently registered devices listed for Invatec S.P.A. include REEF HP 0.035 OTW PTA BALLOON DILATATION CATHETER, ADMIRAL XTREME PTA BALLOON DILATATION CATHETER, SCUBA BILIARY STENT SYSTEM and MO.MA ULTRA PROXIMAL CEREBRAL PROTECTION DEVICE, MODEL MUS0130069X6.