Cdx Corp.
United StatesFDA applicant, unverified
- Devices
- 4
What Cdx Corp. makes
Cdx Corp. manufactures Class II medical devices, including the SUPERSPIRO—a mechanical or implantable device likely used for cardiac rhythm management or structural heart support—and the CDX 200, CXD 400, and CDX80, which appear to be diagnostic or monitoring systems for cardiovascular or respiratory applications.
These devices are regulated under the FDA’s 510(k) pathway as Class II and are listed in the FDA’s 510(k) clearance registry. The company is headquartered in the United States.
Catalogue
Superspiro Ref K853190
Regimes: 510(k) Registry: 510(k)Cdx 200 Ref K820035
Regimes: 510(k) Registry: 510(k)Cxd 400 Ref K820036
Regimes: 510(k) Registry: 510(k)CDX80 Ref K842536
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Cdx Corp. have in the registry?
The registry currently lists 4 devices for Cdx Corp.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Cdx Corp.'s devices?
Among its 4 most recently registered devices, Cdx Corp. has devices listed in FDA 510(k) (4 devices).
What risk classes do Cdx Corp.'s devices fall under?
Among its 4 most recently registered devices, the classes recorded for Cdx Corp.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Cdx Corp. in the registry?
The most recently registered devices listed for Cdx Corp. include SUPERSPIRO, CDX 200, CXD 400 and CDX80.