Calidad Solutions, Inc.
Country not established
- Devices
- 1
What Calidad Solutions, Inc. makes
Calidad Solutions, Inc. manufactures the ACTIVON TULLE, a surgical mesh product designed for use in hernia repair procedures, including inguinal and ventral hernia treatments.
The ACTIVON TULLE is classified as a Class II device under FDA regulations and is listed in the FDA’s 510(k) clearance registry. The company is headquartered in the United States.
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Activon Tulle Ref K101118
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Calidad Solutions, Inc. have in the registry?
The registry currently lists 1 device for Calidad Solutions, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Calidad Solutions, Inc.'s devices?
Among its 1 most recently registered device, Calidad Solutions, Inc. has devices listed in FDA 510(k) (1 device).
What are the newest devices from Calidad Solutions, Inc. in the registry?
The most recently registered devices listed for Calidad Solutions, Inc. include ACTIVON TULLE.