Third Party Review Group
FDA-accredited third party reviewer for expedited 510(k) medical device clearance
Third Party Review Group
FDA-accredited third party reviewer for expedited 510(k) medical device clearance
Best For
Medical device manufacturers seeking expedited FDA 510(k) clearance for eligible devices across anesthesiology, cardiovascular, dental, gastroenterology, neurology, obstetrics/gynecology, ophthalmic, orthopedic, physical medicine, and radiology categories. Well-suited for both established global manufacturers and emerging companies requiring expert regulatory guidance to accelerate time to market.
Location:
Madison, New Jersey, United States
Founded:
2010
Team:
11-50
Certs:
1 verified