Dixon Medical, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Dixon Medical, Inc. - FDA 510(k) Cleared Devices
12
Total
12
Cleared
0
Denied
Dixon Medical, Inc. has 12 FDA 510(k) cleared obstetrics & gynecology devices. Based in Atlanta, US.
Historical record: 12 cleared submissions from 1990 to 1990.
Browse the complete list of FDA 510(k) cleared obstetrics & gynecology devices from this manufacturer. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Dixon Medical, Inc.
12 devices
Cleared
Oct 17, 1990
ESPI DOUBLE-ACTION GRASPER, INSULATED, #8202-N
Obstetrics & Gynecology
70d
Cleared
Oct 17, 1990
ESPI DOUBLE-ACTION INSULATED GRASPER, #8203-N
Obstetrics & Gynecology
70d
Cleared
Oct 17, 1990
ESPI MICRO GRASPER,DOUBLE-ACTION,INSULATED,#8250-N
Obstetrics & Gynecology
70d
Cleared
Sep 12, 1990
ESPI HOOK/UNIVERSAL SCISSORS, # 8101
Obstetrics & Gynecology
35d
Cleared
Sep 12, 1990
ESPI CLAW FORCEP, #8301, 5MM, 30 CM LENGTH
Obstetrics & Gynecology
35d
Cleared
Sep 12, 1990
ESPI APPLICATOR SLEEVE, #8410
Obstetrics & Gynecology
35d
Cleared
Sep 12, 1990
ESPI TISSUE GRASPER/NEEDLE HOLDER, #8201
Obstetrics & Gynecology
35d
Cleared
Sep 12, 1990
ESPI CLAW FORCEP, #8302, 10MM, 30CM
Obstetrics & Gynecology
35d
Cleared
Sep 12, 1990
ESPI REDUCER SLEEVE, #8415
Obstetrics & Gynecology
35d
Cleared
Sep 12, 1990
ESPI MICRO SCISSORS, #8150
Obstetrics & Gynecology
35d
Cleared
Sep 12, 1990
ESPI NON-INSULATED DOUBLE-ACTION GRASPER #8204
Obstetrics & Gynecology
35d
Cleared
Sep 12, 1990
ESPI NON-INSULATED DOUBLE-ACTION GRASPER, #8203
Obstetrics & Gynecology
35d