Medical device makerLabelled 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 13, 2026, FDA's public records list Gemore Technology with 14 510(k) clearances. The most recent is a 510(k) clearance dated Aug 16, 2019: GIM-STIM OTC TENS/EMS System.
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.
| Date | Record | Source |
|---|---|---|
| Aug 16, 2019 | GIM-STIM OTC TENS/EMS SystemK190988 · NUH | 510(k) clearances |
| May 12, 2015 | GEMORE OTC TENSK150681 · NUH | 510(k) clearances |
| Dec 21, 2012 | GEMORE TRUE SINE INTERFERENTIAL STIMULATORK122944 · LIH | 510(k) clearances |
| Dec 21, 2012 | GEM-STIM COMBO STIMULATORK122948 · GZJ | 510(k) clearances |
| Jul 20, 2012 | GEMORE TENS SYSTEMK120569 · GZJ | 510(k) clearances |
| Sep 2, 2011 | GEM-TONE BODY TRAINING SYSTEMK102933 · NGX | 510(k) clearances |
| Aug 25, 2011 | GEMORE MUSCLE CONDITIONER;K102926 · NGX | 510(k) clearances |
| Oct 16, 2009 | GEM-STONE ABDOMINAL TRAINING SYSTEM; MODEL GEM-TONE 310PE/320PE/330PE/340PE/350PE.K091833 · 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
