American Ortomed Corp.
United StatesFDA applicant, unverified
- Devices
- 6
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Titanium Mittelmeier Type Acetabular Ref K842466
Regimes: 510(k) Registry: 510(k)Uniloc-Cementless & Self Tap Acetabular Ref K842518
Regimes: 510(k) Registry: 510(k)The Icr Knee Ref K820719
Regimes: 510(k) Registry: 510(k)Spheristem Total Hip Prosthesis Ref K780497
Regimes: 510(k) Registry: 510(k)Cement Restrictor Ref K840413
Regimes: 510(k) Registry: 510(k)Uniloc Ref K842465
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does American Ortomed Corp. have in the registry?
The registry currently lists 6 devices for American Ortomed Corp.. Devices recorded under merged duplicate company entries are counted once.
Which registries list American Ortomed Corp.'s devices?
Among its 6 most recently registered devices, American Ortomed Corp. has devices listed in FDA 510(k) (6 devices).
What risk classes do American Ortomed Corp.'s devices fall under?
Among its 6 most recently registered devices, the classes recorded for American Ortomed Corp.'s devices are Class II and Class III. Each device page shows its own class and authorisation.
What are the newest devices from American Ortomed Corp. in the registry?
The most recently registered devices listed for American Ortomed Corp. include TITANIUM MITTELMEIER TYPE ACETABULAR, UNILOC-CEMENTLESS & SELF TAP ACETABULAR, THE ICR KNEE and SPHERISTEM TOTAL HIP PROSTHESIS.