American Silk Sutures, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
American Silk Sutures, Inc. - FDA 510(k) Cleared Devices
14
Total
14
Cleared
0
Denied
American Silk Sutures, Inc. has 14 FDA 510(k) cleared medical devices. Based in Ledyard, US.
Historical record: 14 cleared submissions from 1985 to 1992. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by American Silk Sutures, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - American Silk Sutures, Inc.
14 devices
Cleared
Aug 10, 1992
AMERICAN BURN SHEET
General Hospital
96d
Cleared
Mar 27, 1991
STRUNG TELFA NON-ADHERENT SPONGE
Neurology
176d
Cleared
Sep 18, 1990
RAYON NEUROLOGICAL SPONGE
Neurology
77d
Cleared
Dec 04, 1987
STRUNG DENTAL ROLLS
Dental
143d
Cleared
Sep 16, 1987
AMERICAN BRAIN RETRACTOR COVER
General & Plastic Surgery
50d
Cleared
Sep 04, 1987
AMERICAN NASAL SPONGE
Ear, Nose, Throat
42d
Cleared
Aug 11, 1987
SUCTION TUBE TIP FITS OVER BUSSIE FRAZIER TUBE
General & Plastic Surgery
18d
Cleared
Aug 04, 1987
STICK SPONGE, STRUNG TONSIL SPONGE DOUBLE STRUNG
General & Plastic Surgery
21d
Cleared
Aug 04, 1987
NON-WOVEN TRACHEOTOMY SPONGE
General & Plastic Surgery
21d
Cleared
Aug 04, 1987
CHEVRON TAPE DISSECTOR, 9/16 X 1/4, 9/16 X 1/8
General & Plastic Surgery
21d
Cleared
Aug 04, 1987
GAUZE CHERRY SPONGE
General & Plastic Surgery
21d
Cleared
Jul 30, 1986
POLYESTER SPONGE PATTIE
Neurology
29d
Cleared
Mar 20, 1986
COTTON NEUROLOGICAL SPONGE
Neurology
118d
Cleared
Dec 17, 1985
X-RAY DETECTABLE COTTON BALLS
General & Plastic Surgery
25d