# Sonotech, Inc.

- Location (FDA's records): Bellingham, WA
- FDA decisions: 14 (1995–2004): 14 510(k) clearances
- Product codes: ITX (8), MUI (4), IYO (1), GCJ (1)
- Predicates its devices cite: 6 (1 its own); citations of its devices by later devices: 6 (1 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- Sonomed Technology, Inc.: 3 (https://510kreport.com/company/sonomed-technology)
- Johnson & Johnson Professionals, Inc.: 2 (https://510kreport.com/company/johnson-johnson-professionals)

## Firms that cite its devices most
- Farco Pharma GmbH: 2 (https://510kreport.com/company/farco-pharma)
- Sheathing Technologies, Inc.: 1 (https://510kreport.com/company/sheathing-technologies)
- Bard Access Systems, Inc.: 1 (https://510kreport.com/company/bard-access-systems)
- Ob The-Addition, LLC: 1 (https://510kreport.com/company/ob-the-addition)

## Its most-cited devices
- K031894: Scantec Pad (2003), cited by 2
- K042619: Ultrabio - in Vivo Biocompatible, Bioeliminated Sterile Ultrasound Imaging Couplant (2004), cited by 2
- K984562: Vivosonic (1999), cited by 1
- K033178: Ultrabio (2004), cited by 1

## Recent decisions
- K042619: Ultrabio - in Vivo Biocompatible, Bioeliminated Sterile Ultrasound Imaging Couplant (Nov 5, 2004)
- K033178: Ultrabio (Aug 4, 2004)
- K031222: Scanlube (Jul 23, 2003)
- K031894: Scantec Pad (Jul 18, 2003)
- K013701: Endo-Glide (Feb 4, 2002)
- K013170: Scantac Membrane or Scantac Strip (Nov 13, 2001)
- K984562: Vivosonic (Jun 8, 1999)
- K983691: Scanflex Solid Couplant Membrane (May 5, 1999)

Source page: https://510kreport.com/company/sonotech