SCITECK Diagnostics
Also registered as Sciteck Diagnostics, Inc.
United Statesfrom the FDA registration address FDA establishment FEI 3004875840
- Devices
- 5
- Registrations
- FDA
- FDA recalls
- 0
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
- Registry: GUDID
- Registry: GUDID
- Registry: GUDID
- Registry: GUDID
- Regimes: 510(k) Registry: 510(k)
Company details
- FDA FEI number
- 3004875840
- Address
- 317 Rutledge Road, Fletcher, NC, 28732
Frequently asked questions
How many devices does SCITECK Diagnostics have in the registry?
The registry currently lists 5 devices for SCITECK Diagnostics. Devices recorded under merged duplicate company entries are counted once.
Which registries list SCITECK Diagnostics's devices?
Among its 5 most recently registered devices, SCITECK Diagnostics has devices listed in FDA 510(k) (1 device) and FDA GUDID (4 devices). A device can be listed in more than one registry, so these counts overlap.
What risk classes do SCITECK Diagnostics's devices fall under?
Among its 5 most recently registered devices, the classes recorded for SCITECK Diagnostics's devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from SCITECK Diagnostics in the registry?
The most recently registered devices listed for SCITECK Diagnostics include Sciteck AUA-450, AutoUA® 217-S, AutoUA® 200-60 and AutoUA® 200-120.