Scinticor, Inc.
United StatesFDA applicant, unverified
- Devices
- 2
What Scinticor, Inc. makes
Scinticor, Inc. makes medical devices such as the SIM-400 SYSTEM and SYSTEM SEVENTY SEVEN.
The company's portfolio includes devices classified as Class I and Class II, and is listed in the FDA 510(k) registry, with the company based in the US.
Catalogue
Sim-400 System Ref K931193
Regimes: 510(k) Registry: 510(k)System Seventy Seven Ref K885054
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Scinticor, Inc. have in the registry?
The registry currently lists 2 devices for Scinticor, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Scinticor, Inc.'s devices?
Among its 2 most recently registered devices, Scinticor, Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do Scinticor, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Scinticor, Inc.'s devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from Scinticor, Inc. in the registry?
The most recently registered devices listed for Scinticor, Inc. include SIM-400 SYSTEM and SYSTEM SEVENTY SEVEN.