Longwood Valley Medical, Ltd.
ChinaFDA applicant, unverified
- Devices
- 1
What Longwood Valley Medical, Ltd. makes
Longwood Valley Medical, Ltd. develops AIJOINT, a software tool designed for orthopaedic surgery planning that assists in preoperative joint assessment and surgical preparation.
The company’s portfolio is regulated under FDA Class II devices and is listed via the 510(k) pathway. The software is based in the United States.
Catalogue
Orthopaedic Surgery Planning Software (AIJOINT) Ref K233761
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Longwood Valley Medical, Ltd. have in the registry?
The registry currently lists 1 device for Longwood Valley Medical, Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Longwood Valley Medical, Ltd.'s devices?
Among its 1 most recently registered device, Longwood Valley Medical, Ltd. has devices listed in FDA 510(k) (1 device).
What risk classes do Longwood Valley Medical, Ltd.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Longwood Valley Medical, Ltd.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Longwood Valley Medical, Ltd. in the registry?
The most recently registered devices listed for Longwood Valley Medical, Ltd. include Orthopaedic Surgery Planning Software (AIJOINT).