Hanson Medical, Inc. is one of 5120 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Hanson Medical, Inc. - FDA 510(k) Cleared Devices
14
Total
14
Cleared
0
Denied
Hanson Medical, Inc. has 14 FDA 510(k) cleared general & plastic surgery devices. Based in Goleta, US.
Historical record: 14 cleared submissions from 1997 to 2014.
Browse the complete list of FDA 510(k) cleared general & plastic surgery devices from this manufacturer. Filter by specialty or product code using the sidebar.
Hanson Medical, Inc. — FDA 510(k) Products and Clearance History
14 devices
Cleared
Aug 05, 2014
SENSEI X ROBOTIC CATHETER SYSTEM
Cardiovascular
29d
Cleared
Jun 30, 2010
HANSON MEDICAL FACIAL IMPLANTS
General & Plastic Surgery
463d
Cleared
May 25, 2007
MONARCH NASAL IMPLANT
General & Plastic Surgery
45d
Cleared
Feb 11, 2005
MONARCH NASAL IMPLANT
General & Plastic Surgery
234d
Cleared
Aug 12, 2004
HANSON SCAR ADE
General & Plastic Surgery
185d
Cleared
Apr 21, 2003
HANSON MEDICAL CALF IMPLANT
General & Plastic Surgery
39d
Cleared
Apr 21, 2003
HANSON MEDICAL GLUTEAL IMPLANT
General & Plastic Surgery
39d
Cleared
Dec 24, 1997
POWERFLEX PEC IMPLANT
General & Plastic Surgery
85d
Cleared
Dec 24, 1997
DURASIL I AND DURASIL II
General & Plastic Surgery
85d
Cleared
Nov 13, 1997
DURALASTIC ANATOMICAL NASAL IMPLANTS
General & Plastic Surgery
55d
Cleared
Nov 13, 1997
SILICONE CARVING BLOCK
General & Plastic Surgery
44d
Cleared
Nov 07, 1997
DURALASTIC ANATOMICAL CHIN IMPLANTS
General & Plastic Surgery
49d
Cleared
Oct 24, 1997
DURALASTIC ANATOMICAL MALAR IMPLANT
General & Plastic Surgery
35d
Cleared
Oct 21, 1997
KELOCOTE SCAR GEL AND KELOCOTE LASER GEL
General & Plastic Surgery
32d