Company ยท BE
Cefaly Technology
FDA 510(k) clearances and medical device recalls filed under this name, 2016 to 2024. Name variants (Inc, Corp, punctuation) are merged.
6510(k) clearances (0 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)
Product codes
| Code | Device | Records |
|---|---|---|
| PCC | Stimulator, Nerve, Electrical, Transcutaneous, For Migraine | 6 |
Latest 510(k) clearances
| Decided | 510(k) | Device and applicant | Code |
|---|---|---|---|
| Jul 18, 2024 | K234029 | CEFALY Connected - OTC, CEFALY Connected - Rx Cefaly Technology, BE | PCC |
| Dec 13, 2022 | K212071 | Cefaly Dual Enhanced with RFID - OTC, Cefaly Dual Enhanced with RFID - Rx, Cefaly Dual Connected - OTC, Cefaly Dual Conn Cefaly Technology, BE | PCC |
| Sep 29, 2020 | K201895 | Cefaly Dual Cefaly Technology, BE | PCC |
| Nov 28, 2017 | K173006 | Cefaly Dual Cefaly Technology, BE | PCC |
| Sep 15, 2017 | K171446 | Cefaly Acute Cefaly Technology, BE | PCC |
| Mar 4, 2016 | K160237 | Cefaly Cefaly Technology, BE | PCC |
Latest recalls
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| No recalls in this window. | |||