Ideatrics, Inc. is one of 25872 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Ideatrics, Inc. - FDA 510(k) Cleared Devices
Recent clearances: ARAGON WIRING SYSTEM WIRE CARTRIDGE, MODELS I0007 WIRE CARTRIDGE, 22 GAUGE, I0008 WIRE CARTRIDGE, 24 GAUGE, I0009 WIRE E
1
Total
1
Cleared
0
Denied
Ideatrics, Inc. has 1 FDA 510(k) cleared medical devices. Based in Boulder, US.
Historical record: 1 cleared submissions from 2002 to 2002. Primary specialty: Dental.
Browse the FDA 510(k) cleared devices submitted by Ideatrics, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Ideatrics, Inc.
1 devices