Company ยท FR
Bioserenity Sas
FDA 510(k) clearances and medical device recalls filed under this name, 2017 to 2023. Name variants (Inc, Corp, punctuation) are merged.
5510(k) clearances (0 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)
Product codes
Latest 510(k) clearances
| Decided | 510(k) | Device and applicant | Code |
|---|---|---|---|
| Nov 9, 2023 | K231366 | Neuronaute Plus Bioserenity Sas, FR | GWQ |
| Jan 12, 2023 | K223644 | Neuronaute with IceCap 2 & IceCap 2 Small Bioserenity, FR | GWQ |
| Dec 10, 2020 | K202334 | Neuronaute Bioserenity Sas, FR | GWQ |
| Aug 11, 2018 | K173248 | CARDIOSKIN Bioserenity Sas, FR | DXH |
| Dec 26, 2017 | K170138 | NEURONAUTE Bioserenity, FR | GWQ |
Latest recalls
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| No recalls in this window. | |||