The Tiggs Co.
Country not established
- Devices
- 1
What The Tiggs Co. makes
The Tiggs Co. manufactures the Tigges Spinal, a Class I spinal device designed for surgical applications.
The Tigges Spinal is regulated under the FDA’s 510(k) pathway and is listed in the US registry. The company is based in the United States.
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Tigges Spinal Ref K811176
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does The Tiggs Co. have in the registry?
The registry currently lists 1 device for The Tiggs Co.. Devices recorded under merged duplicate company entries are counted once.
Which registries list The Tiggs Co.'s devices?
Among its 1 most recently registered device, The Tiggs Co. has devices listed in FDA 510(k) (1 device).
What risk classes do The Tiggs Co.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for The Tiggs Co.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from The Tiggs Co. in the registry?
The most recently registered devices listed for The Tiggs Co. include TIGGES SPINAL.