G-Flex Europe Sprl

FDA Regulatory Profile

G-Flex Europe Sprl appears in FDA public data with 0 recalls, 2 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on April 3, 2023.

Summary

Total Recalls
0
510(k) Clearances
2
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K222006Sclerotherapy & Endoscopic NeedlesApril 3, 2023
K211909Cysto-Gastro-SetsJune 9, 2022