Ionics Medical Corp.
United StatesFDA applicant, unverified
- Devices
- 2
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Ionics Levante Intervertebral Pillar, Expandable Ref K983667
Regimes: 510(k) Registry: 510(k)- Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Ionics Medical Corp. have in the registry?
The registry currently lists 2 devices for Ionics Medical Corp.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Ionics Medical Corp.'s devices?
Among its 2 most recently registered devices, Ionics Medical Corp. has devices listed in FDA 510(k) (2 devices).
What risk classes do Ionics Medical Corp.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Ionics Medical Corp.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Ionics Medical Corp. in the registry?
The most recently registered devices listed for Ionics Medical Corp. include IONICS LEVANTE INTERVERTEBRAL PILLAR, EXPANDABLE and DYN-ALIF ANTEROLATERAL INTERVERTEBRAL BODY FUSION DEVICE.