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 its name, each linked to the record.
As of Nov 15, 2026, FDA's public records list Mego Afek AC Ltd. with 17 510(k) clearances. The most recent is a 510(k) clearance dated Apr 14, 2022: Amputee Garment for use with Lympha Press Optimal Plus.
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.
| Apr 14, 2022 | Amputee Garment for use with Lympha Press Optimal PlusK214053 · JOW | 510(k) clearances |
| May 15, 2019 | Recovery Pump, 737R (RPX)K190493 · IRP | 510(k) clearances |
| Mar 25, 2019 | Ballancer Gold, 1212K190015 · IRP | 510(k) clearances |
| Feb 27, 2019 | Lympha Press Optimal PlusK182003 · JOW | 510(k) clearances |
| Nov 3, 2017 | Phlebo Press DVT ModelK172277 · JOW | 510(k) clearances |
| May 31, 2017 | Lympha Press Optimal PlusK170658 · JOW | 510(k) clearances |
| Jan 27, 2017 | RP Lite 760RK163280 · IRP | 510(k) clearances |
| May 26, 2015 | Ballancer 505 System, Model 1201-ACK150269 · IRP | 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
