Cosm Medical
CanadaFDA applicant, unverified FDA FEI 3024374351
- Devices
- 3
- Registrations
- FDA
- FDA recalls
- 0
At a glance
Market reach
- United States
- FDA FEI
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
- Registry: GUDID
- Registry: GUDID
Gynethotics™ Pessary Ref K231786
Regimes: 510(k) Registry: 510(k)
Company details
- FDA FEI number
- 3024374351
- Address
- 101 College Street, South Tower, Suites 230-4, 240, 241 and 242, Toronto Ontario
Frequently asked questions
How many devices does Cosm Medical have in the registry?
The registry currently lists 3 devices for Cosm Medical. Devices recorded under merged duplicate company entries are counted once.
Which registries list Cosm Medical's devices?
Among its 3 most recently registered devices, Cosm Medical has devices listed in FDA 510(k) (1 device) and FDA GUDID (2 devices). A device can be listed in more than one registry, so these counts overlap.
What risk classes do Cosm Medical's devices fall under?
Among its 3 most recently registered devices, the classes recorded for Cosm Medical's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Cosm Medical in the registry?
The most recently registered devices listed for Cosm Medical include V-Caliper 1, Gynethotics Patient-Specific and Gynethotics™ Pessary.