Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field. in SingaporeLabelled 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 14, 2026, FDA's public records list Smartmissimo Technologies Pte. Ltd. with 5 510(k) clearances. The most recent is a 510(k) clearance dated Jul 30, 2021: PowerDot PD-01MT2 Muscle Stimulator.
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.
| Jul 30, 2021 | PowerDot PD-01MT2 Muscle StimulatorK210938 · IPF | 510(k) clearances |
| Feb 23, 2021 | PowerDot PD-01MT2 Muscle StimulatorK210269 · IPF | 510(k) clearances |
| Nov 9, 2018 | PowerDot PD-01MTK181759 · IPF | 510(k) clearances |
| Dec 4, 2017 | PowerDot PD-01MK172876 · NGX | 510(k) clearances |
| Sep 30, 2015 | PowerDot(R) PD-01 Muscle Stimulator (with PowerDot(R) Mobile Application)K150078 · NGX | 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
