Miami Eye Technology, Inc.
United StatesFDA applicant, unverified
- Devices
- 6
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Clayman-Parel Capsule Coupeur Ref K841101
Regimes: 510(k) Registry: 510(k)Surgical Iop Monitor Ref K832996
Regimes: 510(k) Registry: 510(k)Abbott Globe Holder Ref K832911
Regimes: 510(k) Registry: 510(k)Rare-Earth Intra-Ocular Magnet Ref K831702
Regimes: 510(k) Registry: 510(k)Epa Automated Infusion Pole Ref K832997
Regimes: 510(k) Registry: 510(k)Gelender Vacuum Fixation Ring Sys Ref K832912
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Miami Eye Technology, Inc. have in the registry?
The registry currently lists 6 devices for Miami Eye Technology, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Miami Eye Technology, Inc.'s devices?
Among its 6 most recently registered devices, Miami Eye Technology, Inc. has devices listed in FDA 510(k) (6 devices).
What risk classes do Miami Eye Technology, Inc.'s devices fall under?
Among its 6 most recently registered devices, the classes recorded for Miami Eye Technology, Inc.'s devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from Miami Eye Technology, Inc. in the registry?
The most recently registered devices listed for Miami Eye Technology, Inc. include CLAYMAN-PAREL CAPSULE COUPEUR, SURGICAL IOP MONITOR, ABBOTT GLOBE HOLDER and RARE-EARTH INTRA-OCULAR MAGNET.