Third Party Review Group Information

Third Party Review Group (TPRG) is one of only a few companies in the world accredited by the US FDA to provide Medical Device 510(K) clearances. Our dedicated Third Party Review team of professionals is comprised of some of the top leaders in the medical device arena with accreditation capabilities covering 7 FDA Office of Device Evaluation Divisions that reach across 13 Device Branches and over 1,200 product codes. With an average of 24 years of US and International industry 510(k) submission experience, our reviewers are poised and ready to meet your company needs. With our main office located in New York City and our recently opened satellite offices in San Diego, CA, and Belfast, Northern Ireland, our reviewers are strategically placed in multiple time zones to satisfy every client need regardless of location.