Medical Device Manufacturer · US , Washington , DC

Xylos Corporation - FDA 510(k) Cleared Devices

9 submissions · 8 cleared · Since 1998

Total

Cleared

Denied

Xylos Corporation has 8 FDA 510(k) cleared medical devices. Based in Washington, US.

Historical record: 8 cleared submissions from 1998 to 2011. Primary specialty: General & Plastic Surgery.

Browse the FDA 510(k) cleared devices submitted by Xylos Corporation Filter by specialty or product code using the sidebar.

Xylos Corporation 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 - Xylos Corporation

9 devices

1-9 of 9

Cleared Aug 25, 2011

XYLOS MACRO-POROUS SURGICAL MESH

K111584 · FTM

General & Plastic Surgery · 79d

XYLOS POROUS SURGICAL MESH

K090880 · FTM

General & Plastic Surgery · 57d

Cleared Apr 28, 2009

MTA PROTECTIVE SHEET

K090778 · FTM

General & Plastic Surgery · 36d

Cleared Mar 18, 2009

SECURIAN TISSUE REINFORCEMENT MATRIX

K083823 · FTM

General & Plastic Surgery · 86d

Cleared Jul 11, 2008

MODIFICATION TO XYLOS SURGICAL MESH

K081882 · FTM

General & Plastic Surgery · 9d

Cleared Mar 18, 2003

XYLOS SURGICAL MESH

K023237 · FTM

General & Plastic Surgery · 172d

Cleared Mar 07, 2003

XYLOS XCELL ANTIMICROBIAL DRESSING

K024054 · MGQ

General & Plastic Surgery · 88d

Cleared Jun 22, 1998

X-CELL WOUND DRESSING

K974251 · MGQ

General & Plastic Surgery · 221d

Xylos Corporation - FDA 510(k) Cleared Devices

FDA 510(k) Regulatory Record - Xylos Corporation

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