ClearanceBrief
Company ยท US

Hanson Medical, Inc.

FDA 510(k) clearances and medical device recalls filed under this name, 1997 to 2014. Name variants (Inc, Corp, punctuation) are merged.

14510(k) clearances (0 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)

Product codes

CodeDeviceRecords
FZEProsthesis, Nose, Internal4
MIBElastomer, Silicone Block4
MDAElastomer, Silicone, For Scar Management2
DXXSystem, Catheter Control, Steerable1
FWPProsthesis, Chin, Internal1
LZKImplant, Malar1
MICImplant, Muscle, Pectoralis1

Latest 510(k) clearances

Decided510(k)Device and applicantCode
Aug 5, 2014K141822SENSEI X ROBOTIC CATHETER SYSTEM
Hanson Medical, Inc.
DXX
Jun 30, 2010K090803HANSON MEDICAL FACIAL IMPLANTS
Hanson Medical, Inc.
FZE
May 25, 2007K071018MONARCH NASAL IMPLANT
Hanson Medical, Inc.
FZE
Feb 11, 2005K041690MONARCH NASAL IMPLANT
Hanson Medical, Inc.
FZE
Aug 12, 2004K040307HANSON SCAR ADE
Hanson Medical, Inc.
MDA
Apr 21, 2003K030809HANSON MEDICAL GLUTEAL IMPLANT
Hanson Medical, Inc.
MIB
Apr 21, 2003K030808HANSON MEDICAL CALF IMPLANT
Hanson Medical, Inc.
MIB
Dec 24, 1997K973730DURASIL I AND DURASIL II
Hanson Medical, Inc.
MIB
Dec 24, 1997K973729POWERFLEX PEC IMPLANT
Hanson Medical, Inc.
MIC
Nov 13, 1997K973728SILICONE CARVING BLOCK
Hanson Medical, Inc.
MIB
Nov 13, 1997K973573DURALASTIC ANATOMICAL NASAL IMPLANTS
Hanson Medical, Inc.
FZE
Nov 7, 1997K973575DURALASTIC ANATOMICAL CHIN IMPLANTS
Hanson Medical, Inc.
FWP
Oct 24, 1997K973574DURALASTIC ANATOMICAL MALAR IMPLANT
Hanson Medical, Inc.
LZK
Oct 21, 1997K973572KELOCOTE SCAR GEL AND KELOCOTE LASER GEL
Hanson Medical, Inc.
MDA

Latest recalls

DateFirm and productCodeLinked 510(k)
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