Saliwell , Ltd. is one of 474 FDA 510(k) medical device manufacturers from Israel in the dataset, ranked by real submission volume.
Saliwell , Ltd. has 4 FDA 510(k) cleared medical devices. Based in Harutzim, IL.
Last cleared in 2023. Active since 2017. Primary specialty: Dental.
Browse the FDA 510(k) cleared devices submitted by Saliwell , Ltd. Filter by specialty or product code using the sidebar.
1 device has linked clinical trial registered on ClinicalTrials.gov.
FDA 510(k) Regulatory Record - Saliwell , Ltd.
4 devices