Medaica, Inc.
United Statesfrom the FDA registration address FDA FEI 3020741819
- Devices
- 1
- Registrations
- FDA
- FDA recalls
- 0
At a glance
Market reach
- United States
- FDA FEI
What Medaica, Inc. makes
Medaica, Inc. manufactures the Medaica M1 Telehealth Stethoscope, a remote diagnostic device designed for auscultation in telemedicine settings.
The company’s portfolio is regulated under FDA Class II devices and includes submissions via the 510(k) pathway. The device is listed in the FDA registry. Medaica, Inc. is based in the United States.
Catalogue
Medaica M1 Telehealth Stethoscope Ref K223166
Regimes: 510(k) Registry: 510(k)
Company details
- FDA FEI number
- 3020741819
- Address
- 170 S Green Valley Pkwy Ste 300, Henderson, NV, 89012
Frequently asked questions
How many devices does Medaica, Inc. have in the registry?
The registry currently lists 1 device for Medaica, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Medaica, Inc.'s devices?
Among its 1 most recently registered device, Medaica, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Medaica, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Medaica, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Medaica, Inc. in the registry?
The most recently registered devices listed for Medaica, Inc. include Medaica M1 Telehealth Stethoscope.