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 Beijing Superlaser Technology with 5 510(k) clearances. The most recent is a 510(k) clearance dated Sep 3, 2025: Diode laser therapy device (VADER).
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.
| Sep 3, 2025 | Diode laser therapy device (VADER)K251457 · GEX | 510(k) clearances |
| Jun 9, 2020 | CO2 Laser SystemK200042 · GEX | 510(k) clearances |
| Apr 13, 2020 | ND:YAG LaserK193464 · GEX | 510(k) clearances |
| Dec 10, 2019 | Diode Laser 808nmK192516 · GEX | 510(k) clearances |
| Nov 27, 2019 | Multi-modality workstationK192519 · ONF | 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
