Alexandria Research Technologies, LLC
United StatesFDA applicant, unverified
- Devices
- 2
What Alexandria Research Technologies, LLC makes
Alexandria Research Technologies, LLC designs modular tibial systems and unicompartmental knee arthroplasty implants for partial knee replacement procedures, including standalone and modular configurations for the tibia.
These devices are classified as Class II under FDA regulations and are listed via the 510(k) pathway. The company is based in the United States.
Catalogue
- Regimes: 510(k) Registry: 510(k)
Tgs Unicompartmental Knee Arthroplasty System Ref K090024
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Alexandria Research Technologies, LLC have in the registry?
The registry currently lists 2 devices for Alexandria Research Technologies, LLC. Devices recorded under merged duplicate company entries are counted once.
Which registries list Alexandria Research Technologies, LLC's devices?
Among its 2 most recently registered devices, Alexandria Research Technologies, LLC has devices listed in FDA 510(k) (2 devices).
What risk classes do Alexandria Research Technologies, LLC's devices fall under?
Among its 2 most recently registered devices, the classes recorded for Alexandria Research Technologies, LLC's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Alexandria Research Technologies, LLC in the registry?
The most recently registered devices listed for Alexandria Research Technologies, LLC include TGS UNICOMPARTMENTAL KNEE ARTHROPLASTY (TGS UKA) MODULAR TIBIA SYSTEM and TGS UNICOMPARTMENTAL KNEE ARTHROPLASTY SYSTEM.