Mego Afek
Mego Afek appears in FDA public data with 0 recalls, 6 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on February 24, 2026.
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 6
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|---|---|
| K254267 | NanoPress 760A-BT (760A-BT) | February 24, 2026 |
| K230385 | Ballancer Platinum (1222) | April 4, 2023 |
| K072372 | PHLEBOPRESS MODEL 601A COMPRESSION THERAPY DEVICE | November 21, 2007 |
| K060220 | PBS MODEL 701A COMPRESSION THERAPY DEVICE | February 9, 2006 |
| K013331 | LYMPHA PRESS PLUS DEVICE | November 30, 2001 |
| K810338 | LYMPHA PRESS | October 20, 1981 |