Bioserenity Sas

FDA Regulatory Profile

Bioserenity Sas appears in FDA public data with 0 recalls, 5 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on November 9, 2023.

Summary

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

Recent 510(k) Clearances

K-NumberDeviceDate
K231366Neuronaute PlusNovember 9, 2023
K223644Neuronaute with IceCap 2 & IceCap 2 SmallJanuary 12, 2023
K202334NeuronauteDecember 10, 2020
K173248CARDIOSKINAugust 11, 2018
K170138NEURONAUTEDecember 26, 2017