Company · FR
Therapixel
FDA 510(k) clearances and medical device recalls filed under this name, 2020 to 2026. Name variants (Inc, Corp, punctuation) are merged.
7510(k) clearances (1 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 |
|---|---|---|---|
| Jun 26, 2026 | K260714 | MammoScreen® (5) Therapixel, FR | QDQ |
| Aug 22, 2025 | K243685 | MammoScreen BD Therapixel, FR | QIH |
| Jul 3, 2025 | K243679 | MammoScreen® (4) Therapixel, FR | QDQ |
| Oct 2, 2024 | K241561 | MammoScreen BD Therapixel, FR | QIH |
| Aug 1, 2024 | K240301 | MammoScreen® (3) Therapixel, FR | QDQ |
| Nov 26, 2021 | K211541 | MammoScreen 2.0 Therapixel, FR | QDQ |
| Mar 25, 2020 | K192854 | MammoScreen Therapixel, FR | QDQ |
Latest recalls
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| No recalls in this window. | |||