Global Manufacturing Technology
Country not established
- Devices
- 3
What Global Manufacturing Technology makes
Global Manufacturing Technology produces modular hip arthroplasty systems, including the MSA HIP SYSTEM and PARAGON HIP SYSTEM, designed for primary and revision total hip replacements. These systems include femoral and acetabular components intended for orthopedic surgeons to address degenerative joint disease and trauma-related hip injuries.
The company’s hip systems are classified as Class II devices under FDA regulations and are authorised via the 510(k) pathway. These products are listed in the FDA’s 510(k) database. The manufacturer operates from the United States.
Catalogue
Msa Hip System Ref K102172
Regimes: 510(k) Registry: 510(k)Paragon Hip System Ref K123782
Regimes: 510(k) Registry: 510(k)Msa Hip System Ref K113107
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Global Manufacturing Technology have in the registry?
The registry currently lists 3 devices for Global Manufacturing Technology. Devices recorded under merged duplicate company entries are counted once.
Which registries list Global Manufacturing Technology's devices?
Among its 3 most recently registered devices, Global Manufacturing Technology has devices listed in FDA 510(k) (3 devices).
What risk classes do Global Manufacturing Technology's devices fall under?
Among its 3 most recently registered devices, the classes recorded for Global Manufacturing Technology's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Global Manufacturing Technology in the registry?
The most recently registered devices listed for Global Manufacturing Technology include MSA HIP SYSTEM and PARAGON HIP SYSTEM.