Xeridiem Medical Devices, A Spectrum Plastics Group Company is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Xeridiem Medical Devices, A Spectrum Plastics Group Company - FDA 510...
Recent clearances: Kangaroo Skin Level Balloon Gastrostomy Kit, Kangaroo Bolus Feed Set with ENFIT Connection, Kangaroo Continuous Feed Set with ENFIT Connection, Entuit LP Gastrostomy BR Low Profile Balloon Retention Feeding Tube, Entuit LP Gastrostomy BR Low Profile Balloon Retention Feeding Tube with ENFit Connection, Entuit LP Patient Care Kit, Entuit LP Patient Care Kit with ENFit Connection, PromaX Low Profile Gastrostomy Feeding Tube, PromaX LP Patient Care Kit with ENFit
2
Total
1
Cleared
0
Denied
Xeridiem Medical Devices, A Spectrum Plastics Group Company has 1 FDA 510(k) cleared medical devices. Based in Tucson, US.
Last cleared in 2023. Active since 2018. Primary specialty: Gastroenterology & Urology.
Browse the FDA 510(k) cleared devices submitted by Xeridiem Medical Devices, A Spectrum Plastics Group Company Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Xeridiem Medical Devices, A Spectrum Plastics Group Company
2 devices