Moist Medical, Inc.
Country not established
- Devices
- 1
What Moist Medical, Inc. makes
Moist Medical, Inc. manufactures the MOIST Punctal Plug System, a device designed for the temporary occlusion of the punctum to retain moisture in the eye and manage dry eye conditions.
The MOIST Punctal Plug System is classified as a Class II (U) device under FDA regulations and is listed in the FDA’s 510(k) clearance registry. The company is based in the United States.
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Moist Punctal Plug System Ref K021936
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Moist Medical, Inc. have in the registry?
The registry currently lists 1 device for Moist Medical, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Moist Medical, Inc.'s devices?
Among its 1 most recently registered device, Moist Medical, Inc. has devices listed in FDA 510(k) (1 device).
What are the newest devices from Moist Medical, Inc. in the registry?
The most recently registered devices listed for Moist Medical, Inc. include MOIST PUNCTAL PLUG SYSTEM.