Anstek Corp.
United StatesFDA applicant, unverified
- Devices
- 2
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
S2MEDIAN Ref K832295
Regimes: 510(k) Registry: 510(k)S2 Posterior-Tib Ref K832296
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Anstek Corp. have in the registry?
The registry currently lists 2 devices for Anstek Corp.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Anstek Corp.'s devices?
Among its 2 most recently registered devices, Anstek Corp. has devices listed in FDA 510(k) (2 devices).
What risk classes do Anstek Corp.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Anstek Corp.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Anstek Corp. in the registry?
The most recently registered devices listed for Anstek Corp. include S2MEDIAN and S2 POSTERIOR-TIB.