Gm Dos Reis Industria E Comerico Ltda. is one of 50 FDA 510(k) medical device manufacturers from Brazil in the dataset, ranked by real submission volume.
Gm Dos Reis Industria E Comerico Ltda. - FDA 510(k) Cleared Devices
Recent clearances: Suture Anchors - HTA Headless Titanium Anchor and Zip Anchors, Mini and Micro Fragments Reconstruction System – GMReis, Pedimax II - Pedicular Screw Spinal System
3
Total
3
Cleared
0
Denied
Gm Dos Reis Industria E Comerico Ltda. has 3 FDA 510(k) cleared medical devices. Based in Campinas, BR.
Last cleared in 2023. Active since 2019. Primary specialty: Orthopedic.
Browse the FDA 510(k) cleared devices submitted by Gm Dos Reis Industria E Comerico Ltda. Filter by specialty or product code using the sidebar.
Regulatory submissions have been managed by Passarini Regulatory Affairs of America, LLC and Pr Servicos Regulatorios Administrativos Ltda.
FDA 510(k) Regulatory Record - Gm Dos Reis Industria E Comerico Ltda.
3 devices