Xeridiem (Formerly Mri) is one of 5098 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Xeridiem (Formerly Mri) - FDA 510(k) Cleared Devices
2
Total
2
Cleared
0
Denied
Xeridiem (Formerly Mri) has 2 FDA 510(k) cleared medical devices. Based in Tucson, US.
Historical record: 2 cleared submissions from 2015 to 2015. Primary specialty: Gastroenterology & Urology.
Browse the FDA 510(k) cleared devices submitted by Xeridiem (Formerly Mri) Filter by specialty or product code using the sidebar.
Xeridiem (Formerly Mri) — FDA 510(k) Products and Clearance History
2 devices
Cleared
Jan 08, 2015
BI-FUNNEL GASTROSTOMY FEEDING TUBE, TRI-FUNNEL GASTROSTOMY FEEDING TUBE
Gastroenterology & Urology
161d
Cleared
Jan 08, 2015
Endo Vive 3S Low Profile Balloon Kit, Endo Vive 3S Bolus Extension Sets, Endo...
Gastroenterology & Urology
143d