Eagle Twe, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Eagle Twe, Inc. - FDA 510(k) Cleared Devices
5
Total
5
Cleared
0
Denied
Eagle Twe, Inc. has 5 FDA 510(k) cleared medical devices. Based in Tucker, US.
Historical record: 5 cleared submissions from 2001 to 2005. Primary specialty: Obstetrics & Gynecology.
Browse the FDA 510(k) cleared devices submitted by Eagle Twe, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Eagle Twe, Inc.
5 devices
Cleared
Aug 19, 2005
DIVAS DUAL PLEASURE MALE LATEX CONDOM
Obstetrics & Gynecology
94d
Cleared
Mar 30, 2001
SHEER THIN AROMAS RED LATEX CONDOM
Obstetrics & Gynecology
86d
Cleared
Mar 29, 2001
SHEER THIN AROMAS YELLOW LATEX CONDOM
Obstetrics & Gynecology
90d
Cleared
Mar 27, 2001
SHEER THIN AROMAS BLUE LATEX CONDOM
Obstetrics & Gynecology
90d
Cleared
Mar 27, 2001
SHEER THIN AROMAS GREEN LATEX CONDOM
Obstetrics & Gynecology
89d