Updoc, Inc.
Country not established
- Devices
- 2
What Updoc, Inc. makes
Updoc, Inc. manufactures the UpDoc, a digital health platform designed to streamline medical documentation and clinical workflows for healthcare providers.
The UpDoc platform is classified as a Class II medical device in the US and is listed under the FDA’s 510(k) pathway. The company is based in the United States.
Catalogue
- GUDID
UpDoc Ref K253281
510(k) 510(k)
Company details
- DUNS number
- 119383564
- [email protected]
- Phone
- 9252125766
Frequently asked questions
How many devices does Updoc, Inc. have in the registry?
The registry currently lists 2 devices for Updoc, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Updoc, Inc.'s devices?
Among its 2 most recently registered devices, Updoc, Inc. has devices listed in FDA 510(k) (1 device) and FDA GUDID (1 device). A device can be listed in more than one registry, so these counts overlap.
What risk classes do Updoc, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Updoc, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Updoc, Inc. in the registry?
The most recently registered devices listed for Updoc, Inc. include UpDoc V1.0 and UpDoc.