Arcon Corp.
United StatesFDA applicant, unverified
- Devices
- 2
What Arcon Corp. makes
Arcon Corp. manufactures the Casablanca, a male external condom designed for barrier contraception and protection against sexually transmitted infections, and the Mentor Plus condom, a lubricated variant of the same product.
The company’s portfolio consists of Class II devices listed under the FDA’s 510(k) pathway, reflecting regulatory clearance for these products. Arcon Corp. is based in the United States.
Catalogue
Casablanca Ref K841600
Regimes: 510(k) Registry: 510(k)Mentor Plus (Condom) Ref K874383
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Arcon Corp. have in the registry?
The registry currently lists 2 devices for Arcon Corp.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Arcon Corp.'s devices?
Among its 2 most recently registered devices, Arcon Corp. has devices listed in FDA 510(k) (2 devices).
What risk classes do Arcon Corp.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Arcon Corp.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Arcon Corp. in the registry?
The most recently registered devices listed for Arcon Corp. include CASABLANCA and MENTOR PLUS (CONDOM).