Medical Device Manufacturer · US , Largo , FL

Smith & Nephew United, Inc. - FDA 510(k) Cleared Devices

34 submissions · 23 cleared · Since 1989

Total

Cleared

Denied

Smith & Nephew United, Inc. has 23 FDA 510(k) cleared general & plastic surgery devices. Based in Largo, US.

Historical record: 23 cleared submissions from 1989 to 1996.

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.

Smith & Nephew United, 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 - Smith & Nephew United, Inc.

34 devices

1-12 of 34

Cleared Oct 25, 1996

ALLEVYN HYDRO POLY DRESSING ND ALL TRAC DRESSING

K963096 · KMF

General & Plastic Surgery · 77d

Cleared Jul 16, 1996

PROFORE FOUR-LAYER BANDAGE SYSTEM KIT

K961775 · EFQ

General & Plastic Surgery · 69d

Cleared Feb 09, 1995

ALLEVYN ADHESIVE

K945330 · KMF

General & Plastic Surgery · 100d

Cleared Aug 19, 1994

CAVI-CARE CONFORMING FOAM DRESSING

K943619 · KMF

General & Plastic Surgery · 23d

Cleared Jun 29, 1994

INTRASITE

K942748 · NAE

General & Plastic Surgery · 19d

Cleared Feb 15, 1994

ALLEVYN ISLAND WOUND DRESSING

K935705 · NAE

General & Plastic Surgery · 77d

Cleared Feb 03, 1994

CICA-CARE SILICONE GEL SHEET

K935803 · MDA

General & Plastic Surgery · 63d

Cleared Oct 01, 1993

SOLOSITE DERMAL WOUND GEL

K932263 · MGQ

General & Plastic Surgery · 164d

Cleared Jul 13, 1993

INTRASITE GEL

K926508 · NAE

General & Plastic Surgery · 195d

Cleared Sep 15, 1992

STRAPPAL

K922897 · KGX

General & Plastic Surgery · 91d

Cleared Feb 03, 1992

ALLEVLYN WOUND DRESSING, MODIFICATION

K914147 · KMF

General & Plastic Surgery · 140d

Cleared Jan 09, 1992

REMOVE ADHESIVE REMOVER

K915150 · KOX

General & Plastic Surgery · 56d

Smith & Nephew United, Inc. - FDA 510(k) Cleared Devices

FDA 510(k) Regulatory Record - Smith & Nephew United, Inc.

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