Corinthian Medical, Ltd.
NetherlandsFDA applicant, unverified
- Devices
- 1
What Corinthian Medical, Ltd. makes
Corinthian Medical, Ltd. manufactures the SERENOCEM (Model BC 010), a medical device designed for the treatment of varicose veins using a sclerotherapy technique with a proprietary foam formulation.
The SERENOCEM is classified as a Class II device under FDA regulations and is listed in the FDA’s 510(k) clearance registry. The company is based in the United States.
Catalogue
Serenocem, Model Bc 010 Ref K003567
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Corinthian Medical, Ltd. have in the registry?
The registry currently lists 1 device for Corinthian Medical, Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Corinthian Medical, Ltd.'s devices?
Among its 1 most recently registered device, Corinthian Medical, Ltd. has devices listed in FDA 510(k) (1 device).
What risk classes do Corinthian Medical, Ltd.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Corinthian Medical, Ltd.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Corinthian Medical, Ltd. in the registry?
The most recently registered devices listed for Corinthian Medical, Ltd. include SERENOCEM, MODEL BC 010.