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 Wuhan Lotuxs Technology with 5 510(k) clearances. The most recent is a 510(k) clearance dated Jan 30, 2024: DermRays Revive.
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.
| Jan 30, 2024 | DermRays ReviveK231910 · GEX | 510(k) clearances |
| Nov 28, 2023 | Diode Laser Hair Removal (LHR-V6S-1064, LHR-V6S/B-1064)K232117 · GEX | 510(k) clearances |
| Apr 19, 2023 | Diode Laser Hair RemovalK230090 · OHT | 510(k) clearances |
| Jul 17, 2019 | Powersculp laser lipolysis systemK191068 · PKT | 510(k) clearances |
| Jul 1, 2015 | SILKPRO laser hair removal systemK142845 · OHT | 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
