Ascend Eagle, Inc. is one of 20536 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Ascend Eagle, Inc. - FDA 510(k) Cleared Devices
Recent clearances: NON-STERILE POWDER- FREE PEACH COLOR, NITRILE EXAMINATION GLOVES WITH LANO-E AND PEPPERMINT CITRUS SCENT, NON STERILE POWDER-FREE, NATURAL OR AQUA LANO-E NITRILE EXAMINATION GLOVES, WITH OR WITHOUT CITRUS/ PEPPERMINT SCENT, NON-STERILE POWDER FREE NATURAL/GREEN LANO-E LATEX EXAM GLOVES, WITH OR WIHOUT CITRUS/PEPPERMINT SCENT PLUS A PROTEIN
3
Total
3
Cleared
0
Denied
Ascend Eagle, Inc. has 3 FDA 510(k) cleared medical devices. Based in American Canyon, US.
Historical record: 3 cleared submissions from 2006 to 2010. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Ascend Eagle, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Ascend Eagle, Inc.
3 devices
Cleared
Oct 15, 2010
NON-STERILE POWDER- FREE PEACH COLOR, NITRILE EXAMINATION GLOVES WITH LANO-E...
General Hospital
154d
Cleared
Apr 15, 2010
NON STERILE POWDER-FREE, NATURAL OR AQUA LANO-E NITRILE EXAMINATION GLOVES,...
General Hospital
246d
Cleared
Jan 25, 2006
NON-STERILE POWDER FREE NATURAL/GREEN LANO-E LATEX EXAM GLOVES, WITH OR...
General Hospital
120d