ClearanceBrief
Company ยท US

Xylos Corporation

FDA 510(k) clearances and medical device recalls filed under this name, 1998 to 2011. Name variants (Inc, Corp, punctuation) are merged.

9510(k) clearances (0 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)

Product codes

CodeDeviceRecords
FTMMesh, Surgical6
MGQDressing, Wound And Burn, Hydrogel W/Drug And/Or Biologic2
OMRVessel Guard Or Cover1

Latest 510(k) clearances

Decided510(k)Device and applicantCode
Aug 25, 2011K111584XYLOS MACRO-POROUS SURGICAL MESH
Xylos Corporation
FTM
Jul 7, 2010K100984XYLOS VESSEL GUARD
Xylos Corporation
OMR
May 27, 2009K090880XYLOS POROUS SURGICAL MESH
Xylos Corporation
FTM
Apr 28, 2009K090778MTA PROTECTIVE SHEET
Xylos Corporation
FTM
Mar 18, 2009K083823SECURIAN TISSUE REINFORCEMENT MATRIX
Xylos Corporation
FTM
Jul 11, 2008K081882MODIFICATION TO XYLOS SURGICAL MESH
Xylos Corporation
FTM
Mar 18, 2003K023237XYLOS SURGICAL MESH
Xylos Corporation
FTM
Mar 7, 2003K024054XYLOS XCELL ANTIMICROBIAL DRESSING
Xylos Corporation
MGQ
Jun 22, 1998K974251X-CELL WOUND DRESSING
Xylos Corporation
MGQ

Latest recalls

DateFirm and productCodeLinked 510(k)
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