Ahava Stein
IsraelFDA applicant, unverified
- Devices
- 1
What Ahava Stein makes
Ahava Stein manufactures pneumatic peripheral circulation improvement devices, specifically footrest systems designed to enhance blood flow in peripheral circulation.
These devices are classified as Class II under FDA regulations and are listed via the 510(k) pathway. The company is based in the United States.
Catalogue
- Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Ahava Stein have in the registry?
The registry currently lists 1 device for Ahava Stein. Devices recorded under merged duplicate company entries are counted once.
Which registries list Ahava Stein's devices?
Among its 1 most recently registered device, Ahava Stein has devices listed in FDA 510(k) (1 device).
What risk classes do Ahava Stein's devices fall under?
Among its 1 most recently registered device, the classes recorded for Ahava Stein's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Ahava Stein in the registry?
The most recently registered devices listed for Ahava Stein include PPCID- PNEUMATIC PERIPHERAL CIRCULATION IMPROVEMENT (FOOTREST) DEVICE.