Hanson Medical, Inc.
Hanson Medical, Inc. holds FDA 510(k) medical device clearances, first cleared 1997, most recent 2014.
Top product codes for Hanson Medical, Inc.
Recent clearances by Hanson Medical, Inc.
- K141822 — SENSEI X ROBOTIC CATHETER SYSTEM
- K090803 — HANSON MEDICAL FACIAL IMPLANTS
- K071018 — MONARCH NASAL IMPLANT
- K041690 — MONARCH NASAL IMPLANT
- K040307 — HANSON SCAR ADE
- K030808 — HANSON MEDICAL CALF IMPLANT
- K030809 — HANSON MEDICAL GLUTEAL IMPLANT
- K973729 — POWERFLEX PEC IMPLANT
- K973730 — DURASIL I AND DURASIL II
- K973573 — DURALASTIC ANATOMICAL NASAL IMPLANTS
- K973728 — SILICONE CARVING BLOCK
- K973575 — DURALASTIC ANATOMICAL CHIN IMPLANTS
- K973574 — DURALASTIC ANATOMICAL MALAR IMPLANT
- K973572 — KELOCOTE SCAR GEL AND KELOCOTE LASER GEL
Data sourced from openFDA. This site is unofficial and independent of the FDA.