Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field. in IsraelLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field.. FDA records under 2 spellings of its name, each linked to the record.
As of Nov 15, 2026, FDA's public records list Mego Afek with 6 510(k) clearances. The most recent is a 510(k) clearance dated Feb 24, 2026: NanoPress 760A-BT (760A-BT).
Drug approvals, 510(k) clearances, recalls and letters, 2017 to 2026 to date
A hatched bar is a year that is not over, so its count covers only part of the year.
| Feb 24, 2026 | NanoPress 760A-BT (760A-BT)K254267 · JOW | 510(k) clearances |
| Apr 4, 2023 | Ballancer Platinum (1222)K230385 · IRP | 510(k) clearances |
| Nov 21, 2007 | PHLEBOPRESS MODEL 601A COMPRESSION THERAPY DEVICEK072372 · JOW | 510(k) clearances |
| Feb 9, 2006 | PBS MODEL 701A COMPRESSION THERAPY DEVICEK060220 · JOW | 510(k) clearances |
| Nov 30, 2001 | LYMPHA PRESS PLUS DEVICEK013331 · JOW | 510(k) clearances |
| Oct 20, 1981 | LYMPHA PRESSK810338 · JOW | 510(k) clearances |
Spellings are joined only when they reduce to the same name, or a reviewed source names the same company. Sharing an FDA establishment number (FEI) is not enough: contract sites make products for many firms. Facts marked AI were labelled by a language model from the firm's FDA names; everything else comes from FDA or Wikidata. How this page is built
