Zevex, Inc.

FDA Regulatory Profile

Zevex, Inc. appears in FDA public data with 0 recalls, 5 510(k) clearances, 7 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on October 3, 2024.

Summary

Total Recalls
0
510(k) Clearances
5
Inspections
7
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K242660Curlin 8000 Ambulatory Infusion System; Enterprise Solution (ES) Software; Curlin 380-series AdminisOctober 3, 2024
K232793Curlin 8000 Ambulatory Infusion System; Enterprise Solution (ES) Software; Curlin 380-Series AdminstMay 17, 2024
K142539EnteraLite Infinity Enteral Pump Delivery Set, 1200 mL Enteral Feeding Delivery SetJanuary 8, 2015
K131154ENTERALITE INFINITY SPIKE ENTERAL DELIVERY SET; ENTERALITE INFINITY 500 ML BAG ENTERAL DELIVERY SET;February 12, 2014
K012147DEVICE MODIFICATION OF ENTERAL FEEDING SETS FOR GRAVITY AND PUMP USENovember 2, 2001