Visant Medical, Inc.
Country not established
- Devices
- 1
What Visant Medical, Inc. makes
Visant Medical, Inc. manufactures the Visant Medical Canalicular Plug, a device designed for placement in the canaliculus to manage ocular drainage issues.
The Canalicular Plug 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
Visant Medical Canalicular Plug Ref K222164
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Visant Medical, Inc. have in the registry?
The registry currently lists 1 device for Visant Medical, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Visant Medical, Inc.'s devices?
Among its 1 most recently registered device, Visant Medical, Inc. has devices listed in FDA 510(k) (1 device).
What are the newest devices from Visant Medical, Inc. in the registry?
The most recently registered devices listed for Visant Medical, Inc. include Visant Medical Canalicular Plug.