VanDuzen, Inc. dba MedCAD
Also registered as Vanduzen Dba Medcad
United Statesfrom the FDA registration address FDA establishment FEI 3009196021
- Devices
- 1
- Registrations
- FDA
- FDA recalls
- 0
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
- Regimes: 510(k) Registry: 510(k)
Company details
- FDA FEI number
- 3009196021
- Address
- 501 S 2nd Ave Ste A1000, Dallas, TX, 75226
Frequently asked questions
How many devices does VanDuzen, Inc. dba MedCAD have in the registry?
The registry currently lists 1 device for VanDuzen, Inc. dba MedCAD. Devices recorded under merged duplicate company entries are counted once.
Which registries list VanDuzen, Inc. dba MedCAD's devices?
Among its 1 most recently registered device, VanDuzen, Inc. dba MedCAD has devices listed in FDA 510(k) (1 device).
What risk classes do VanDuzen, Inc. dba MedCAD's devices fall under?
Among its 1 most recently registered device, the classes recorded for VanDuzen, Inc. dba MedCAD's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from VanDuzen, Inc. dba MedCAD in the registry?
The most recently registered devices listed for VanDuzen, Inc. dba MedCAD include MEDCAD ACCUSHAPE (TM) PEEK PATIENT SPECIFIC CRANIAL / CRANIOFACIAL IMPLANT.