Pelican Bay Kel-Cor
Country not established
- Devices
- 1
What Pelican Bay Kel-Cor makes
Pelican Bay Kel-Cor manufactures the Pelican Bay Kel-Cor Cephalometric System, a device used for capturing and analyzing lateral cephalograms in orthodontics and maxillofacial assessments.
The company’s portfolio is regulated under FDA’s Class I device classification, with the Pelican Bay Kel-Cor Cephalometric System listed in the FDA’s 510(k) clearance registry. The manufacturer is based in the United States.
Catalogue
Pelican Bay Kel-Cor Cephalometric Sys. Ref K791916
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Pelican Bay Kel-Cor have in the registry?
The registry currently lists 1 device for Pelican Bay Kel-Cor. Devices recorded under merged duplicate company entries are counted once.
Which registries list Pelican Bay Kel-Cor's devices?
Among its 1 most recently registered device, Pelican Bay Kel-Cor has devices listed in FDA 510(k) (1 device).
What risk classes do Pelican Bay Kel-Cor's devices fall under?
Among its 1 most recently registered device, the classes recorded for Pelican Bay Kel-Cor's devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Pelican Bay Kel-Cor in the registry?
The most recently registered devices listed for Pelican Bay Kel-Cor include PELICAN BAY KEL-COR CEPHALOMETRIC SYS..