Artiglass Srl

FDA Regulatory Profile

Artiglass Srl appears in FDA public data with 0 recalls, 2 510(k) clearances, 1 FDA inspection, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on May 19, 2022.

Summary

Total Recalls
0
510(k) Clearances
2
Inspections
1
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K213800Artiglass NRFitTM Tip L.O.R. Glass SyringesMay 19, 2022
K122416ARTIGLASS L. O.R. GLASS SYRINGEMay 3, 2013