Dualtek, Inc.
Country not established
- Devices
- 1
What Dualtek, Inc. makes
Dualtek, Inc. manufactures the CHANNEL-EDGE BRACKET SYSTEM, a Class I orthopedic fixation device designed for spinal stabilization procedures.
The CHANNEL-EDGE BRACKET SYSTEM is listed under the FDA’s 510(k) pathway and is based in the United States.
Catalogue
Channel-Edge Bracket System Ref K930881
510(k) 510(k)
Frequently asked questions
How many devices does Dualtek, Inc. have in the registry?
The registry currently lists 1 device for Dualtek, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Dualtek, Inc.'s devices?
Among its 1 most recently registered device, Dualtek, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Dualtek, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Dualtek, Inc.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Dualtek, Inc. in the registry?
The most recently registered devices listed for Dualtek, Inc. include CHANNEL-EDGE BRACKET SYSTEM.