S. Jackson, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
S. Jackson, Inc. - FDA 510(k) Cleared Devices
16
Total
16
Cleared
0
Denied
S. Jackson, Inc. has 16 FDA 510(k) cleared general & plastic surgery devices. Based in Mchenry, US.
Historical record: 16 cleared submissions from 1980 to 2008.
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 - S. Jackson, Inc.
16 devices
Cleared
Sep 15, 2008
SUPRAMESH EXTRA
General & Plastic Surgery
230d
Cleared
Sep 25, 1997
STERILE SUPRAFOIL SMOOTH NYLON FOIL SHEETS
General & Plastic Surgery
17d
Cleared
Dec 17, 1993
NYLAMID SUTURE
General & Plastic Surgery
260d
Cleared
Dec 17, 1993
SUPRAMID SUTURE
General & Plastic Surgery
260d
Cleared
Dec 17, 1993
MOPYLEN SUTURE
General & Plastic Surgery
260d
Cleared
Oct 20, 1992
MOPYLEN
General & Plastic Surgery
139d
Cleared
Oct 02, 1991
N80-838 SUPRAMID EXTRA SUTURE
General & Plastic Surgery
124d
Cleared
Oct 25, 1990
SUPRAMID EXTRA SUTURES
General & Plastic Surgery
57d
Cleared
Jun 11, 1985
NYLAMID MESH PAD FULL & HALF
General & Plastic Surgery
46d
Cleared
Aug 16, 1983
FOIL IN 3 FORMS-NON-STERILE SHEETS
General & Plastic Surgery
77d
Cleared
Aug 12, 1983
SUPRAMID EXTRA SURGICAL MESH
General & Plastic Surgery
73d
Cleared
Aug 12, 1983
CHIN (MENTOPLASTY) IMPLANTS
General & Plastic Surgery
73d
Cleared
Aug 12, 1983
QUARTER GLOBE CAPS
General & Plastic Surgery
73d
Cleared
Aug 11, 1983
EYE MUSCLE SLEEVES
General & Plastic Surgery
72d
Cleared
Jan 18, 1982
SHARTPOINT EYED NEEDLES
General & Plastic Surgery
21d
Cleared
Dec 10, 1980
JACKSON HYDRO SYSTEM
General Hospital
35d