MINNEAPOLIS--(BUSINESS WIRE)--Medspira announces a multi-center randomized clinical trial utilizing an investigational biofeedback device (based on the FDA cleared and currently marketed mcompass ...
Medspira has announced it has received FDA 510(k) clearance for its mcompass anorectal manometry device, according to a news release. The device, which evaluates pelvic floor function in patients with ...
Brighter Health Network and Medspira are partnering to further market, distribute and service Medspira’s mcompass anorectal manometry system. 1. Brighter Health Network is a medical diagnostics ...
Some results have been hidden because they may be inaccessible to you
Show inaccessible results