TOKYO, Aug. 30, 2023 /PRNewswire/ — BionicM, an innovative Japanese medical device startup, is pleased to announce that it has received U.S. Food and Drug Administration (FDA) 510(k) exemption registration for Bio Leg™; its robotic prosthetic knee. This registration marks a significant…
![](http://box5750.temp.domains/~legalte4/wp-content/uploads/2019/01/PRimage.jpg)
BionicM Earns FDA Registration and Class II Exempt Device Listing for Bio Leg™; Its New Motor-Robotic Prosthetic Knee
This post was originally published on this site