# Sightline Technologies, Ltd.

- Location (FDA's records): Matam, Haifa, IL
- FDA decisions: 3 (2000–2004): 3 510(k) clearances
- Product codes: FER (2), FDF (1)
- Predicates its devices cite: 8 (1 its own); citations of its devices by later devices: 7 (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
- Vision-Sciences, Inc.: 4 (https://510kreport.com/company/vision-sciences)
- Pentax Precision Instrument Corp.: 3 (https://510kreport.com/company/pentax-precision-instrument)

## Firms that cite its devices most
- Neoguide Systems, Inc.: 2 (https://510kreport.com/company/neoguide-systems)
- Stryker GI: 1 (https://510kreport.com/company/stryker-gi)
- Sheathing Technologies, Inc.: 1 (https://510kreport.com/company/sheathing-technologies)
- Invendo Medical Gbmh: 1 (https://510kreport.com/company/invendo-medical-gbmh)
- Easyglide, Ltd.: 1 (https://510kreport.com/company/easyglide)

## Its most-cited devices
- K032688: Colonosight Model 510B (2004), cited by 6
- K994130: Rectosight RS 300-04 (2000), cited by 1

## Recent decisions
- K032688: Colonosight Model 510B (Mar 5, 2004)
- K011825: Rectosight RS300-04;and Protosight PS300-04 Device (Jul 11, 2001)
- K994130: Rectosight RS 300-04 (Jun 30, 2000)

Source page: https://510kreport.com/company/sightline-technologies