Flowmedic, Ltd.
IsraelFDA applicant, unverified
- Devices
- 2
What Flowmedic, Ltd. makes
Flowmedic, Ltd. manufactures the AVIAFIT, a non-invasive leg compression device, and the AVIAFIT Pulsating Legband, designed for intermittent pneumatic compression therapy to support venous circulation and reduce swelling in the lower limbs.
These devices are classified as Class II under FDA regulations and are listed via the 510(k) clearance process. The company is based in the United States.
Catalogue
Aviafit Ref K111720
Regimes: 510(k) Registry: 510(k)Aviafit Pulsating Legband Ref K071744
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Flowmedic, Ltd. have in the registry?
The registry currently lists 2 devices for Flowmedic, Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Flowmedic, Ltd.'s devices?
Among its 2 most recently registered devices, Flowmedic, Ltd. has devices listed in FDA 510(k) (2 devices).
What risk classes do Flowmedic, Ltd.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Flowmedic, Ltd.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Flowmedic, Ltd. in the registry?
The most recently registered devices listed for Flowmedic, Ltd. include AVIAFIT and AVIAFIT PULSATING LEGBAND.