Crosstex
Country not established
- Devices
- 1
What Crosstex makes
Crosstex manufactures external indicators for medical containers, including label and card-based solutions designed to improve visibility and tracking of sterile supplies.
These products are regulated as Class II devices under FDA 510(k) clearance requirements and are listed in the FDA’s 510(k) database. The company is based in the United States.
Catalogue
SPSmedical VH202 External Indicator (Container Cards), SPSmedical VH202 External Indicator (Label) Ref K143520
510(k) 510(k)
Frequently asked questions
How many devices does Crosstex have in the registry?
The registry currently lists 1 device for Crosstex. Devices recorded under merged duplicate company entries are counted once.
Which registries list Crosstex's devices?
Among its 1 most recently registered device, Crosstex has devices listed in FDA 510(k) (1 device).
What risk classes do Crosstex's devices fall under?
Among its 1 most recently registered device, the classes recorded for Crosstex's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Crosstex in the registry?
The most recently registered devices listed for Crosstex include SPSmedical VH202 External Indicator (Container Cards), SPSmedical VH202 External Indicator (Label).