Eradlink, Inc.
United StatesFDA 510(k) applicant, unverified
- Devices
- 2
What Eradlink, Inc. makes
Eradlink, Inc. makes medical devices such as the CR-PRO and LASERPRO 16.
The company's portfolio, which includes Class II devices, is listed in the FDA 510(k) registry, and Eradlink, Inc. is based in the US.
Catalogue
Cr-Pro Ref K052938
510(k) 510(k)Laserpro 16 Ref K020243
510(k) 510(k)
Frequently asked questions
How many devices does Eradlink, Inc. have in the registry?
The registry currently lists 2 devices for Eradlink, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Eradlink, Inc.'s devices?
Among its 2 most recently registered devices, Eradlink, Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do Eradlink, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Eradlink, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Eradlink, Inc. in the registry?
The most recently registered devices listed for Eradlink, Inc. include CR-PRO and LASERPRO 16.