Medical Device Manufacturer · GB , Ruabon, Wrexham

Sutures , Ltd. - FDA 510(k) Cleared Devices

11 submissions · 1 cleared · Since 1987

Recent clearances: SURGISORB

Total

Cleared

Denied

Sutures , Ltd. has 1 FDA 510(k) cleared general & plastic surgery devices. Based in Ruabon, Wrexham, GB.

Historical record: 1 cleared submissions from 1987 to 1999.

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.

Sutures , Ltd. is one of 245 FDA 510(k) medical device manufacturers from United Kingdom in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Sutures , Ltd.

11 devices

1-11 of 11

Cleared May 27, 1999

SURGISORB

K990432 · GAM

General & Plastic Surgery · 105d

Cleared Jan 31, 1996

PRODEK

K953609 · GAW

General & Plastic Surgery · 182d

Cleared Dec 05, 1994

SURGIDEK

K943216 · GAR

General & Plastic Surgery · 153d

Cleared Dec 05, 1994

PLAIN CATGUT

K943217 · GAL

General & Plastic Surgery · 153d

Cleared Dec 05, 1994

CHROMIC CATGUT

K943218 · GAL

General & Plastic Surgery · 153d

Cleared Dec 05, 1994

SUTULENE

K943220 · GAT

General & Plastic Surgery · 153d

Cleared Dec 05, 1994

SURGIBOND

K943221 · GAT

General & Plastic Surgery · 153d

Cleared Dec 05, 1994

SURGIDEK S

K943222 · GAR

General & Plastic Surgery · 153d

Cleared Dec 05, 1994

SURGIDEK B

K943223 · GAR

General & Plastic Surgery · 153d

Cleared Dec 05, 1994

SURGISILK

K943627 · GAP

General & Plastic Surgery · 132d

Cleared Jun 30, 1987

SURGISTEEL

K865038 · GAQ

General & Plastic Surgery · 188d

Sutures , Ltd. - FDA 510(k) Cleared Devices

FDA 510(k) Regulatory Record - Sutures , Ltd.

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