Flexicath, Ltd.
IsraelFDA applicant, unverified
- Devices
- 4
What Flexicath, Ltd. makes
Flexicath, Ltd. manufactures peripherally inserted catheter devices, including firm-grip variants for secure placement, and pressure-injectable catheters designed for imaging applications. Their portfolio includes specialized catheters like the SNM FIRMGRIP, intended for nuclear medicine procedures.
These devices are classified as Class II under FDA regulations and are listed via 510(k) clearance. The company operates from the United States.
Catalogue
Firmgrip Peripherally Inserted Catheter Device Ref K063363
Regimes: 510(k) Registry: 510(k)Firmgrip Ref K080793
Regimes: 510(k) Registry: 510(k)M/29TM - Pressure Injectable Ref K111939
Regimes: 510(k) Registry: 510(k)Snm Firmgrip Ref K092629
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Flexicath, Ltd. have in the registry?
The registry currently lists 4 devices for Flexicath, Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Flexicath, Ltd.'s devices?
Among its 4 most recently registered devices, Flexicath, Ltd. has devices listed in FDA 510(k) (4 devices).
What risk classes do Flexicath, Ltd.'s devices fall under?
Among its 4 most recently registered devices, the classes recorded for Flexicath, Ltd.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Flexicath, Ltd. in the registry?
The most recently registered devices listed for Flexicath, Ltd. include FIRMGRIP PERIPHERALLY INSERTED CATHETER DEVICE, FIRMGRIP, M/29TM - PRESSURE INJECTABLE and SNM FIRMGRIP.