Silimed, LLC is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Silimed, LLC - FDA 510(k) Cleared Devices
9
Total
9
Cleared
0
Denied
Silimed, LLC has 9 FDA 510(k) cleared medical devices. Based in Crofton, US.
Historical record: 9 cleared submissions from 1998 to 1998. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Silimed, LLC Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Silimed, LLC
9 devices
Cleared
Aug 05, 1998
SILIMED VAGINAL STENT
Obstetrics & Gynecology
252d
Cleared
Aug 05, 1998
SILIMED TISSUE EXPANDER
General & Plastic Surgery
71d
Cleared
Jul 09, 1998
SILIMED MALAR IMPLANT
General & Plastic Surgery
44d
Cleared
Jul 09, 1998
SILIMED CHIN IMPLANTS
General & Plastic Surgery
44d
Cleared
Jul 09, 1998
SILIMED SILICONE CARVING BLOCK
General & Plastic Surgery
44d
Cleared
Jun 26, 1998
SILIMED NASAL L SHAPED IMPLANT
General & Plastic Surgery
31d
Cleared
Apr 02, 1998
SILIMED NASAL RETAINER
Ear, Nose, Throat
70d
Cleared
Feb 24, 1998
SILIMED CALF IMPLANT
General & Plastic Surgery
90d
Cleared
Feb 24, 1998
SILIMED GLUTEAL IMPLANT
General & Plastic Surgery
90d