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 Shenzhen Leaflife Technology with 7 510(k) clearances. The most recent is a 510(k) clearance dated Nov 25, 2025: LeafPure-Echo (LM-LPNdA).
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.
| Nov 25, 2025 | LeafPure-Echo (LM-LPNdA)K253219 · GEX | 510(k) clearances |
| Aug 14, 2025 | WinForth (LM-E470KA)K250916 · PBX | 510(k) clearances |
| Feb 20, 2024 | Mjolnir Pro. (Multi–electrode plasma)K233760 · QVJ | 510(k) clearances |
| Sep 11, 2023 | Planar LED mateK230362 · OHT | 510(k) clearances |
| Apr 12, 2022 | LED Therapy Device (Planar LED/Planar LED mini)K220103 · GEX | 510(k) clearances |
| Nov 19, 2021 | Leaf SmoothK212697 · OHT | 510(k) clearances |
| Nov 19, 2020 | Laser Therapy DeviceK202980 · GEX | 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
