Dgimed Ortho, Inc.
United StatesFDA applicant, unverified
- Devices
- 3
What Dgimed Ortho, Inc. makes
Dgimed Ortho, Inc. manufactures intramedullary nail systems designed for orthopedic fixation, including the Distalock Femoral Intramedullary Nail System, the Revolution Femoral Intramedullary Nail System, and the Distalock Tibial IM Nail System.
These devices are classified as Class II medical devices and are listed in the FDA 510(k) database. The company is based in the United States.
Catalogue
Distalock Femoral Intramedullary Nail System Ref K100312
Regimes: 510(k) Registry: 510(k)- Regimes: 510(k) Registry: 510(k)
Distalock Tibial Im Nail System Ref K132830
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Dgimed Ortho, Inc. have in the registry?
The registry currently lists 3 devices for Dgimed Ortho, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Dgimed Ortho, Inc.'s devices?
Among its 3 most recently registered devices, Dgimed Ortho, Inc. has devices listed in FDA 510(k) (3 devices).
What risk classes do Dgimed Ortho, Inc.'s devices fall under?
Among its 3 most recently registered devices, the classes recorded for Dgimed Ortho, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Dgimed Ortho, Inc. in the registry?
The most recently registered devices listed for Dgimed Ortho, Inc. include DISTALOCK FEMORAL INTRAMEDULLARY NAIL SYSTEM, REVOLUTION FEMORAL INTRAMEDULLARY NAIL SYSTEM, MODEL DGOOXX and DISTALOCK TIBIAL IM NAIL SYSTEM.