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Hanson Medical, Inc.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
14
Inspections
2
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K141822SENSEI X ROBOTIC CATHETER SYSTEMAugust 5, 2014
K090803HANSON MEDICAL FACIAL IMPLANTSJune 30, 2010
K071018MONARCH NASAL IMPLANTMay 25, 2007
K041690MONARCH NASAL IMPLANTFebruary 11, 2005
K040307HANSON SCAR ADEAugust 12, 2004
K030808HANSON MEDICAL CALF IMPLANTApril 21, 2003
K030809HANSON MEDICAL GLUTEAL IMPLANTApril 21, 2003
K973730DURASIL I AND DURASIL IIDecember 24, 1997
K973729POWERFLEX PEC IMPLANTDecember 24, 1997
K973728SILICONE CARVING BLOCKNovember 13, 1997
K973573DURALASTIC ANATOMICAL NASAL IMPLANTSNovember 13, 1997
K973575DURALASTIC ANATOMICAL CHIN IMPLANTSNovember 7, 1997
K973574DURALASTIC ANATOMICAL MALAR IMPLANTOctober 24, 1997
K973572KELOCOTE SCAR GEL AND KELOCOTE LASER GELOctober 21, 1997