Eastmed, Inc.
CanadaFDA applicant, unverified
- Devices
- 2
What Eastmed, Inc. makes
Eastmed, Inc. manufactures the URESTA pessary and a modification to the URESTA pessary, both of which are medical devices.
These devices are classified as Class II and are listed in the FDA 510(k) registry. Eastmed, Inc. is based in the US.
Catalogue
Modification To Uresta Pessary Ref K083769
Regimes: 510(k) Registry: 510(k)Uresta Pessary Ref K081385
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Eastmed, Inc. have in the registry?
The registry currently lists 2 devices for Eastmed, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Eastmed, Inc.'s devices?
Among its 2 most recently registered devices, Eastmed, Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do Eastmed, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Eastmed, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Eastmed, Inc. in the registry?
The most recently registered devices listed for Eastmed, Inc. include MODIFICATION TO URESTA PESSARY and URESTA PESSARY.