Dambrecine, Inc.
Country not established
- Devices
- 1
What Dambrecine, Inc. makes
Dambrecine, Inc. manufactures spinal implants and instrumentation under its SPINE LINE, including devices designed for spinal stabilization and fusion procedures.
The company’s portfolio is regulated under FDA Class I devices, with products listed via the 510(k) pathway. The manufacturer is based in the United States.
Catalogue
Spine Line Ref K922366
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Dambrecine, Inc. have in the registry?
The registry currently lists 1 device for Dambrecine, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Dambrecine, Inc.'s devices?
Among its 1 most recently registered device, Dambrecine, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Dambrecine, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Dambrecine, Inc.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Dambrecine, Inc. in the registry?
The most recently registered devices listed for Dambrecine, Inc. include SPINE LINE.