Condax, LLC
United StatesFDA applicant, unverified
- Devices
- 2
What Condax, LLC makes
Condax, LLC makes male condom applicators, including the Kwikeze Male Condom Applicator and the Zeus Male Condom Applicator.
These devices are classified as Class II medical devices and are listed in the FDA 510(k) registry; the company is based in the United States.
Catalogue
Kwikeze Male Condom Applicator Ref K031007
Regimes: 510(k) Registry: 510(k)Zeus Male Condom Applicator Ref K052206
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Condax, LLC have in the registry?
The registry currently lists 2 devices for Condax, LLC. Devices recorded under merged duplicate company entries are counted once.
Which registries list Condax, LLC's devices?
Among its 2 most recently registered devices, Condax, LLC has devices listed in FDA 510(k) (2 devices).
What risk classes do Condax, LLC's devices fall under?
Among its 2 most recently registered devices, the classes recorded for Condax, LLC's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Condax, LLC in the registry?
The most recently registered devices listed for Condax, LLC include KWIKEZE MALE CONDOM APPLICATOR and ZEUS MALE CONDOM APPLICATOR.