FDA applicant
Sightline Technologies, Ltd.
FDA records 3 decisions for Sightline Technologies, Ltd. (Matam, Haifa, IL) from 2000 to 2004: 3 510(k) clearances. Most are in product codes FER (Anoscope And Accessories) and FDF (Colonoscope And Accessories, Flexible/Rigid). Its devices cite 8 predicates, 1 of them its own earlier devices. No recall is linked to its devices.
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) refreshed weekly
How often FDA has decided Sightline Technologies, Ltd.’s devices, and how often a recall has named them.
FDA decisions per year
No FDA decision for Sightline Technologies, Ltd. since 2007.
Recalls per year
No recall linked to its devices since 2007.
Planning a device like Sightline Technologies, Ltd.’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.
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