Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field. in ChinaLabelled 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 Everyway Medical Instruments and its 1 subsidiaries with 31 510(k) clearances. The most recent is a 510(k) clearance dated Nov 21, 2025: Li-Battery Powered OTC TENS/EMS Combination Stimulator, Model Z4.
Drug approvals, 510(k) clearances, recalls and letters, 2017 to 2026 to date, Everyway Medical Instruments and its 1 subsidiaries
A hatched bar is a year that is not over, so its count covers only part of the year.
| Nov 21, 2025 | Li-Battery Powered OTC TENS/EMS Combination Stimulator, Model Z4K251856 · NUH | 510(k) clearances |
| Nov 15, 2022 | Everyway Analog OTC TENSK222488 · NUH | 510(k) clearances |
| Dec 3, 2021 | Everyway Incontinence Stimulation SystemK213116 · KPI | 510(k) clearances |
| Dec 22, 2020 | Everyway Analog OTC TENS, model N103A/N302K202849 · NUH | 510(k) clearances |
| Nov 25, 2020 | Li-Battery powered OTC TENS/EMS, model EM-6000, EM-6100, EM-6200 & EM-6300K202470 · NUH | 510(k) clearances |
| Nov 13, 2020 | Li-Battery powered OTC TENS/EMS, model EV-804, model EV-805, & model EV-806K202317 · NUH | 510(k) clearances |
| Oct 24, 2020 | Li-Battery powered OTC TENS/EMS Combination StimulatorK201335 · NUH | 510(k) clearances |
| Dec 19, 2019 | Everyway OTC TENS/EMS CombinationK192589 · NUH | 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
