Mego Afek
Country not established
- Devices
- 6
What Mego Afek makes
Mego Afek manufactures pneumatic compression therapy devices, including the LYMPHA PRESS, PBS Model 701A, PHLEBOPRESS Model 601A, and LYMPHA PRESS PLUS, designed for lymphatic and venous circulation support. The Ballancer Platinum (1222) is a device intended for balancing and supporting limb circulation. These products are intended for medical use in managing edema and promoting venous return.
The company’s devices are classified as Class II under FDA regulations and are listed via the 510(k) pathway. These products are registered in the U.S. and comply with applicable U.S. medical device standards.
Catalogue
Lympha Press Ref K810338
Regimes: 510(k) Registry: 510(k)Pbs Model 701A Compression Therapy Device Ref K060220
Regimes: 510(k) Registry: 510(k)NanoPress 760A-BT (760A-BT) Ref K254267
Regimes: 510(k) Registry: 510(k)- Regimes: 510(k) Registry: 510(k)
Lympha Press Plus Device Ref K013331
Regimes: 510(k) Registry: 510(k)Ballancer Platinum (1222) Ref K230385
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Mego Afek have in the registry?
The registry currently lists 6 devices for Mego Afek. Devices recorded under merged duplicate company entries are counted once.
Which registries list Mego Afek's devices?
Among its 6 most recently registered devices, Mego Afek has devices listed in FDA 510(k) (6 devices).
What risk classes do Mego Afek's devices fall under?
Among its 6 most recently registered devices, the classes recorded for Mego Afek's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Mego Afek in the registry?
The most recently registered devices listed for Mego Afek include LYMPHA PRESS, PBS MODEL 701A COMPRESSION THERAPY DEVICE, NanoPress 760A-BT (760A-BT) and PHLEBOPRESS MODEL 601A COMPRESSION THERAPY DEVICE.