# Techdevice Corporation

- Location (FDA's records): Watertown, MA
- FDA decisions: 4 (2006–2011): 4 510(k) clearances
- Product codes: DQX (2), MJN (1), OCY (1)
- Predicates its devices cite: 9 (1 its own); citations of its devices by later devices: 5 (1 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
- Boston Scientific Corp: 7 (https://510kreport.com/company/boston-scientific)
- Hitachi Medical Corp.: 1 (https://510kreport.com/company/hitachi-medical)

## Firms that cite its devices most
- Cardiosolutions, Inc.: 2 (https://510kreport.com/company/cardiosolutions)
- Vadiswire Corporation: 1 (https://510kreport.com/company/vadiswire)
- Sonostik, LLC: 1 (https://510kreport.com/company/sonostik)

## Its most-cited devices
- K053251: Techdevice Guidewire (2006), cited by 3
- K110241: Endologix Guidewire (2011), cited by 1
- K051137: Techdevice Occlusion Balloon Catheter (2006), cited by 1

## Recent decisions
- K110241: Endologix Guidewire (Feb 25, 2011)
- K053251: Techdevice Guidewire (Mar 8, 2006)
- K051137: Techdevice Occlusion Balloon Catheter (Feb 24, 2006)
- K053028: Techdevice Guidewire (Jan 31, 2006)

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