Sil-Med Corp. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Sil-Med Corp. - FDA 510(k) Cleared Devices
29
Total
28
Cleared
0
Denied
Sil-Med Corp. has 28 FDA 510(k) cleared general & plastic surgery devices. Based in Mchenry, US.
Historical record: 28 cleared submissions from 1980 to 1997.
Browse the complete list of FDA 510(k) cleared general & plastic surgery devices from this manufacturer. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Sil-Med Corp.
29 devices
Cleared
Oct 01, 1997
NAVIGATOR (STYLET) 2006
General & Plastic Surgery
86d
Cleared
Jul 18, 1997
ANTIMICROBIAL PERITONEAL DIALYSIS COIL CATHETER WITH SPI-ARGENT II
Gastroenterology & Urology
463d
Cleared
Aug 08, 1996
ANTIMICROBIAL MEDIASTINAL SILICONE DRAIN
General & Plastic Surgery
134d
Cleared
Jun 26, 1996
SAPPHIRE LINE FLAT DRAIN/KIT WITH SPI-ARGENT II W/OR W/OUT TROCAR
General & Plastic Surgery
83d
Cleared
Mar 11, 1996
PENROSE DRAIN MODELS 6001 - 6007
General & Plastic Surgery
60d
Cleared
Jan 23, 1996
GRIP-A-BOOTS
General & Plastic Surgery
55d
Cleared
Jan 04, 1996
MEDIASTINAL SILICONE DRAINS
General & Plastic Surgery
575d
Cleared
May 24, 1995
SIL-SLIP (COATED/REGULAR(NON-COATED)THORACIC DRAIN
General & Plastic Surgery
876d
Cleared
Feb 02, 1994
SIL-SLIP FLAT SUCTION DRAIN
General & Plastic Surgery
408d
Cleared
Feb 02, 1994
SIL-SLIP ROUND WOUND DRAIN (COATED)/BLUE STRIPE
General & Plastic Surgery
400d
Cleared
Sep 28, 1992
SIL-MED FLAT SUCTION DRAIN
General & Plastic Surgery
188d
Cleared
Jan 31, 1991
SIL-MED T-TUBE DRAIN
Obstetrics & Gynecology
155d