Hanson Medical, Inc.
FDA 510(k) medical device clearances.
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.