# Hanson Medical, Inc.

- Location (FDA's records): Kingston, WA
- FDA decisions: 14 (1997–2014): 14 510(k) clearances
- Product codes: MIB (4), FZE (4), MDA (2), DXX (1), LZK (1), MIC (1), FWP (1)
- Predicates its devices cite: 8 (3 its own); citations of its devices by later devices: 4 (3 its own)
- Recalls linked to its devices: 1 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- Allied Biomedical Corp.: 3 (https://510kreport.com/company/allied-biomedical)
- Hansen Medical, Inc.: 1 (https://510kreport.com/company/hansen-medical)
- Spirit Ridge Technologies: 1 (https://510kreport.com/company/spirit-ridge-technologies)

## Firms that cite its devices most
- Pillar Surgical, Inc.: 1 (https://510kreport.com/company/pillar-surgical)

## Its most-cited devices
- K973574: Duralastic Anatomical Malar Implant (1997), cited by 1
- K973572: Kelocote Scar Gel and Kelocote Laser Gel (1997), cited by 1
- K973573: Duralastic Anatomical Nasal Implants (1997), cited by 1
- K973575: Duralastic Anatomical Chin Implants (1997), cited by 1

## Recent decisions
- K141822: Sensei X Robotic Catheter System (Aug 5, 2014)
- K090803: Hanson Medical Facial Implants (Jun 30, 2010)
- K071018: Monarch Nasal Implant (May 25, 2007)
- K041690: Monarch Nasal Implant (Feb 11, 2005)
- K040307: Hanson Scar Ade (Aug 12, 2004)
- K030808: Hanson Medical Calf Implant (Apr 21, 2003)
- K030809: Hanson Medical Gluteal Implant (Apr 21, 2003)
- K973730: Durasil I and Durasil II (Dec 24, 1997)

Source page: https://510kreport.com/company/hanson-medical