Meditrina, Inc.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
5
Inspections
2
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K223813Aveta System 2.0August 21, 2023
K213171Aveta System, Aveta Disposable Hysteroscope (Pearl/Opal/Coral), Aveta Disposable Cystoscope (Coral)May 26, 2022
K192100Aveta Disposable HysteroscopeDecember 19, 2019
K191958Aveta SystemOctober 1, 2019
K190372Aveta SystemMay 16, 2019