Canton Medical, Inc.
Country not established
- Devices
- 1
What Canton Medical, Inc. makes
Canton Medical, Inc. manufactures the PRIA-KIT™, a sterile single-use device designed for the treatment of priapism, a prolonged and often painful erection unrelated to sexual stimulation.
The company’s portfolio is regulated under FDA’s Class I device classification, with the PRIA-KIT™ authorised via a 510(k) pathway. The manufacturer is based in the United States.
Catalogue
Pria-Kit (Tm) Priapism Kit S.S. Ref K874000
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Canton Medical, Inc. have in the registry?
The registry currently lists 1 device for Canton Medical, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Canton Medical, Inc.'s devices?
Among its 1 most recently registered device, Canton Medical, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Canton Medical, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Canton Medical, Inc.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Canton Medical, Inc. in the registry?
The most recently registered devices listed for Canton Medical, Inc. include PRIA-KIT (TM) PRIAPISM KIT S.S..