# Linemaster Switch Corp.

- Location (FDA's records): Woodstock, CT
- FDA decisions: 1 (2006–2006): 1 510(k) clearance
- Product codes: GEI (1)
- Predicates its devices cite: 5 (0 its own); citations of its devices by later devices: 4 (0 its own)
- Recalls linked to its devices: 2 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- Applied Surgical, LLC: 1 (https://510kreport.com/company/applied-surgical)
- Stryker Endoscopy: 1 (https://510kreport.com/company/stryker-endoscopy)
- Power Medical Interventions, Inc.: 1 (https://510kreport.com/company/power-medical-interventions)
- Megadyne Medical Products, Inc.: 1 (https://510kreport.com/company/megadyne-medical-products)
- Valleylab, Inc.: 1 (https://510kreport.com/company/valleylab)

## Firms that cite its devices most
- Conmed Linvatec: 1 (https://510kreport.com/company/conmed-linvatec)
- Iridex Corp: 1 (https://510kreport.com/company/iridex)
- Depuy Mitek, A Johnson & Johnson Company: 1 (https://510kreport.com/company/depuy-mitek-a-johnson-johnson)
- Megadyne Medical Products, Inc.: 1 (https://510kreport.com/company/megadyne-medical-products)

## Its most-cited devices
- K053510: IR Wireless Foot Switch (2006), cited by 4

## Recent decisions
- K053510: IR Wireless Foot Switch (Mar 20, 2006)

Source page: https://510kreport.com/company/linemaster-switch