Cooper Surgical is one of 16294 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Cooper Surgical - FDA 510(k) Cleared Devices
Recent clearances: Milex™ Incontinence Dish Pessaries, TEN-YEAR FRACTURE RISK OPTION AND SIRI TABLE OPTION FOR NORLAND DXA BONE DENSITOMETERS, COOPERSURGICAL MALLEABLE SYTLET
6
Total
6
Cleared
0
Denied
Cooper Surgical has 6 FDA 510(k) cleared medical devices. Based in Huntington, US.
Latest FDA clearance: Jan 2026. Active since 2002. Primary specialty: Obstetrics & Gynecology.
Browse the FDA 510(k) cleared devices submitted by Cooper Surgical Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Cooper Surgical
6 devices
Cleared
Jan 20, 2026
Milex™ Incontinence Dish Pessaries
Obstetrics & Gynecology
57d
Cleared
Jun 29, 2009
TEN-YEAR FRACTURE RISK OPTION AND SIRI TABLE OPTION FOR NORLAND DXA BONE...
Radiology
55d
Cleared
Dec 20, 2002
COOPERSURGICAL MALLEABLE SYTLET
Obstetrics & Gynecology
73d
Cleared
Dec 13, 2002
COOPERSURGICAL INTRAUTERINE INSEMINATION CATHETER
Obstetrics & Gynecology
66d
Cleared
Dec 13, 2002
COOPERSURGICAL TRIAL TRANSFER CATHETER
Obstetrics & Gynecology
66d
Cleared
Dec 11, 2002
COOPERSURGICAL EMBRYO TRANSFER CATHETER, COOPERSURGICAL ASSISTED REPRODUCTION...
Obstetrics & Gynecology
64d