Neomedix Corp. - FDA 510(k) Cleared Devices
Recent clearances: TRABECTOME HIGH FREQUENCY GENERATOR/LP, NMX-1000, SUPRAFLOW CONSOLE
4
Total
4
Cleared
0
Denied
FDA 510(k) Regulatory Record - Neomedix Corp. General & Plastic Surgery ✕
4 devices
Cleared
May 18, 2006
TRABECTOME HIGH FREQUENCY GENERATOR/LP
General & Plastic Surgery
13d
Cleared
Apr 22, 2004
NMX-1000
General & Plastic Surgery
48d
Cleared
Feb 17, 2004
SUPRAFLOW CONSOLE
General & Plastic Surgery
15d
Cleared
Feb 25, 2003
MICROSURGICAL BIPOLAR HANDPIECE
General & Plastic Surgery
63d