Medcad
United Statesfrom the FDA registration address FDA FEI 3021635140
- Devices
- 346
- Registrations
- FDA
- FDA recalls
- 0
At a glance
Market reach
- United States
- FDA FEI
Catalogue
Search and filter all 346 devicesShowing 1-50 of 346
Company details
- FDA FEI number
- 3021635140
- DUNS number
- 144723868
- Address
- 3401 Technology Dr, Plano, TX, 75074
- support@medcad.com
- Phone
- (214) 453-8864
Frequently asked questions
How many devices does Medcad have in the registry?
The registry currently lists 346 devices for Medcad. Devices recorded under merged duplicate company entries are counted once.
Which registries list Medcad's devices?
Among its 50 most recently registered devices, Medcad has devices listed in FDA GUDID (50 devices).
What risk classes do Medcad's devices fall under?
Among its 50 most recently registered devices, the classes recorded for Medcad's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Medcad in the registry?
The most recently registered devices listed for Medcad include AccuPlan System MC-KFIT, AccuPlan System MC-3D217, AccuPlan System MC-3D218 and AccuStride System MC-STP001.