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Xeridiem Medical Devices, A Spectrum Plastics Group Company

Tucson, AZ, US

Xeridiem Medical Devices, A Spectrum Plastics Group Company appears in FDA device records in Tucson, AZ. FDA records list 2 510(k) clearances between and , no PMA records and no registered establishments. As of , FDA records show no recalls for this company.

FDA records held for this company

510(k) clearances
2
PMA records
0
Recall records
0
Registered establishments
0

510(k) clearance history

FDA records hold 2 510(k) clearances for Xeridiem Medical Devices, A Spectrum Plastics Group Company between 2018 and 2023. The busiest year on record is 2018, with 1. The most recent is 2023, with 1.

Clearances by year, as a table
510(k) clearance decisions for Xeridiem Medical Devices, A Spectrum Plastics Group Company, by decision year
YearClearances
20181
20231
510(k) clearances on record, most recent first
K numberDeviceProduct codeDecisionDecision date
K232046Kangaroo Skin Level Balloon Gastrostomy Kit, Kangaroo Bolus Feed Set with ENFIT Connection, Kangaroo Continuous Feed Set with ENFIT ConnectionPIFSubstantially Equivalent
K180708Entuit 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 ENFitPIFUnknown

Registered establishments

No FDA establishment registrations recorded against this company.

FDA product codes

Recall records

No recall records for this company in the ingested FDA data.

Verification record

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Data as of , FDA export datePage updated Source: openFDA, public domain