Medical Device Manufacturer · US , Mchenry , IL

S. Jackson, Inc. - FDA 510(k) Cleared Devices

16 submissions · 16 cleared · Since 1980

Total

Cleared

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.

S. Jackson, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - S. Jackson, Inc.

16 devices

1-12 of 16

Cleared Sep 15, 2008

SUPRAMESH EXTRA

K080216 · FTL

General & Plastic Surgery · 230d

Cleared Sep 25, 1997

STERILE SUPRAFOIL SMOOTH NYLON FOIL SHEETS

K973379 · FTM

General & Plastic Surgery · 17d

Cleared Dec 17, 1993

NYLAMID SUTURE

K931612 · GAR

General & Plastic Surgery · 260d

Cleared Dec 17, 1993

SUPRAMID SUTURE

K931613 · GAR

General & Plastic Surgery · 260d

Cleared Dec 17, 1993

MOPYLEN SUTURE

K931614 · GAW

General & Plastic Surgery · 260d

Cleared Oct 20, 1992

MOPYLEN

K922630 · GAW

General & Plastic Surgery · 139d

Cleared Oct 02, 1991

N80-838 SUPRAMID EXTRA SUTURE

K912429 · GAR

General & Plastic Surgery · 124d

Cleared Oct 25, 1990

SUPRAMID EXTRA SUTURES

K904052 · GAR

General & Plastic Surgery · 57d

Cleared Jun 11, 1985

NYLAMID MESH PAD FULL & HALF

K852011 · FTM

General & Plastic Surgery · 46d

Cleared Aug 16, 1983

FOIL IN 3 FORMS-NON-STERILE SHEETS

K831725 · FTM

General & Plastic Surgery · 77d

Cleared Aug 12, 1983

SUPRAMID EXTRA SURGICAL MESH

K831723 · FTM

General & Plastic Surgery · 73d

Cleared Aug 12, 1983

CHIN (MENTOPLASTY) IMPLANTS

K831724 · FWP

General & Plastic Surgery · 73d

S. Jackson, Inc. - FDA 510(k) Cleared Devices

FDA 510(k) Regulatory Record - S. Jackson, Inc.

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