Alleva Medical Devices
United Statesfrom the FDA registration address FDA establishment FEI 3021767551
- Devices
- 2
- Registrations
- FDA
- FDA recalls
- 0
What Alleva Medical Devices makes
Alleva Medical Devices manufactures negative pressure wound therapy systems, including the extriCARE® 1000 and extriCARE® 3000, designed for managing acute and chronic wounds through controlled suction therapy.
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)
- Regimes: 510(k) Registry: 510(k)
Company details
- FDA FEI number
- 3021767551
- Address
- 3101 Pomona Blvd, Pomona, CA, 91768
Frequently asked questions
How many devices does ALLEVA MEDICAL DEVICES have in the registry?
The registry currently lists 2 devices for ALLEVA MEDICAL DEVICES. Devices recorded under merged duplicate company entries are counted once.
Which registries list ALLEVA MEDICAL DEVICES's devices?
Among its 2 most recently registered devices, ALLEVA MEDICAL DEVICES has devices listed in FDA 510(k) (2 devices).
What risk classes do ALLEVA MEDICAL DEVICES's devices fall under?
Among its 2 most recently registered devices, the classes recorded for ALLEVA MEDICAL DEVICES's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from ALLEVA MEDICAL DEVICES in the registry?
The most recently registered devices listed for ALLEVA MEDICAL DEVICES include extriCARE® 1000 Negative Pressure Wound Therapy System and extriCARE® 3000 Negative Wound Pressure Therapy System.