Medlogic Global Corp. is one of 12989 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Medlogic Global Corp. - FDA 510(k) Cleared Devices
Recent clearances: LIQUIBAND DENTAL, SUPERSKIN
2
Total
2
Cleared
0
Denied
Medlogic Global Corp. has 2 FDA 510(k) cleared medical devices. Based in Washington, US.
Historical record: 2 cleared submissions from 1997 to 2000. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Medlogic Global Corp. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Medlogic Global Corp.
2 devices