Medical Device Manufacturer · US , Washington , DC

Xylos Corporation - FDA 510(k) Cleared Devices

9 submissions · 8 cleared · Since 1998

9

Total

8

Cleared

0

Denied

FDA 510(k) Regulatory Record - Xylos Corporation General & Plastic Surgery ✕

8 devices

1-8 of 8

Cleared Aug 25, 2011

XYLOS MACRO-POROUS SURGICAL MESH

General & Plastic Surgery · 79d

Cleared May 27, 2009

XYLOS POROUS SURGICAL MESH

General & Plastic Surgery · 57d

Cleared Apr 28, 2009

MTA PROTECTIVE SHEET

General & Plastic Surgery · 36d

Cleared Mar 18, 2009

SECURIAN TISSUE REINFORCEMENT MATRIX

General & Plastic Surgery · 86d

Cleared Jul 11, 2008

MODIFICATION TO XYLOS SURGICAL MESH

General & Plastic Surgery · 9d

Cleared Mar 18, 2003

XYLOS SURGICAL MESH

General & Plastic Surgery · 172d

Cleared Mar 07, 2003

XYLOS XCELL ANTIMICROBIAL DRESSING

General & Plastic Surgery · 88d

Cleared Jun 22, 1998

X-CELL WOUND DRESSING

General & Plastic Surgery · 221d