Inmed Ltda. is one of 25720 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Inmed Ltda. - FDA 510(k) Cleared Devices
Recent clearances: CSF400 AND CSF600, LEKTROGEL, MODEL LK3001, ULTRAEKOGEL MODELS EK 2000 & EK 2001
3
Total
3
Cleared
0
Denied
Inmed Ltda. has 3 FDA 510(k) cleared medical devices. Based in Alpharetta, US.
Historical record: 3 cleared submissions from 2003 to 2003. Primary specialty: Neurology.
Browse the FDA 510(k) cleared devices submitted by Inmed Ltda. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Inmed Ltda.
3 devices