Shanghai Iatrical-Ti Technologies CO, Ltd.
ChinaFDA applicant, unverified
- Devices
- 1
What Shanghai Iatrical-Ti Technologies CO, Ltd. makes
The company manufactures spinal fusion systems for lumbar interbody procedures, including anterior (ALIF), transforaminal (TLIF), and lateral (LLIF) approaches.
These devices are classified as Class II under FDA regulations and are listed via the 510(k) pathway. The company is based in the US.
Catalogue
- Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Shanghai Iatrical-Ti Technologies CO, Ltd. have in the registry?
The registry currently lists 1 device for Shanghai Iatrical-Ti Technologies CO, Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Shanghai Iatrical-Ti Technologies CO, Ltd.'s devices?
Among its 1 most recently registered device, Shanghai Iatrical-Ti Technologies CO, Ltd. has devices listed in FDA 510(k) (1 device).
What risk classes do Shanghai Iatrical-Ti Technologies CO, Ltd.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Shanghai Iatrical-Ti Technologies CO, Ltd.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Shanghai Iatrical-Ti Technologies CO, Ltd. in the registry?
The most recently registered devices listed for Shanghai Iatrical-Ti Technologies CO, Ltd. include Iatrical Interbody Lumbar Fusion Systems (Model ALIF, Model TLIF, Model LLIF).