Specialty Surgical Products, Inc. is one of 5120 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Specialty Surgical Products, Inc. - FDA 510(k) Cleared Devices
12
Total
12
Cleared
0
Denied
Specialty Surgical Products, Inc. has 12 FDA 510(k) cleared general & plastic surgery devices. Based in Victor, US.
Historical record: 12 cleared submissions from 1997 to 2014.
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.
Specialty Surgical Products, Inc. — FDA 510(k) Products and Clearance History
12 devices
Cleared
Oct 28, 2014
ALLOX2 TISSUE EXPANDERS
General & Plastic Surgery
256d
Cleared
Feb 12, 1999
MAMMARY SIZER, MAMMARY PROTHESIS SIZER
General & Plastic Surgery
87d
Cleared
Feb 05, 1999
VIRILIS PENILE PROSTHESIS
Gastroenterology & Urology
161d
Cleared
Sep 08, 1998
MAMMARY SIZER
General & Plastic Surgery
74d
Cleared
Aug 12, 1998
STERILE SILICONE EXTERNAL WOUND COVER
General & Plastic Surgery
61d
Cleared
Jul 13, 1998
MAGNETIC PORT SILICONE TISSUE EXPANDER
General & Plastic Surgery
31d
Cleared
Mar 13, 1998
SILICONE ELASTOMER SHEETING
General & Plastic Surgery
88d
Cleared
Feb 24, 1998
SILICONE BLOCKS
General & Plastic Surgery
71d
Cleared
Feb 06, 1998
SILICONE TISSUE/INFLATABLE TISSUE EXPANDER
General & Plastic Surgery
88d
Cleared
Nov 18, 1997
DISPOSABLE SILICONE EPISTAXIS CATHETER
Ear, Nose, Throat
54d
Cleared
Nov 04, 1997
VENTRAL WALL DEFECT REDUCTION SILO
General & Plastic Surgery
78d
Cleared
Sep 19, 1997
SILICONE BILIARY STENT/BILIARY CATHETER
Gastroenterology & Urology
30d