Myhomedoc, Ltd.
IsraelFDA applicant, unverified
- Devices
- 1
What Myhomedoc, Ltd. makes
MyHomeDoc, Ltd. manufactures a telehealth platform designed for remote patient monitoring and virtual consultations, enabling healthcare providers to conduct secure video visits and manage patient data digitally.
The company’s portfolio is regulated under FDA Class II devices and includes products listed via the 510(k) clearance pathway. The platform is based in the United States.
Catalogue
MyHomeDoc Ref K202483
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Myhomedoc, Ltd. have in the registry?
The registry currently lists 1 device for Myhomedoc, Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Myhomedoc, Ltd.'s devices?
Among its 1 most recently registered device, Myhomedoc, Ltd. has devices listed in FDA 510(k) (1 device).
What risk classes do Myhomedoc, Ltd.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Myhomedoc, Ltd.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Myhomedoc, Ltd. in the registry?
The most recently registered devices listed for Myhomedoc, Ltd. include MyHomeDoc.