Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field.. FDA records under 2 spellings of its name, each linked to the record.
As of Nov 13, 2026, FDA's public records list Fuji Dynamics with 12 510(k) clearances. The most recent is a 510(k) clearance dated Jul 12, 2016: Fuji Dynamics Incontinence Stimulation Electrode, Models Fuji – 01/ 02/ 03/ 04/ 05/ 06/ ….
| Date | Record | Source |
|---|---|---|
| Jul 12, 2016 | Fuji Dynamics Incontinence Stimulation Electrode, Models Fuji – 01/ 02/ 03/ 04/ 05/ 06/ 07/ 08/ 09/ 10/ 11/ 12/ 13/ 14/ 15K161055 · KPI | 510(k) clearances |
| Jan 22, 2016 | FD TENS 2090, FD TENS 2095K152676 · GZJ | 510(k) clearances |
| Jan 13, 2016 | LL TENS 160A, LL TENS 160BK152374 · NUH | 510(k) clearances |
| Mar 1, 2012 | FD TENS 2070K111654 · GZJ | 510(k) clearances |
| Nov 9, 2011 | FD TENS 2050 OR SLIDE TENS MODEL FD2050K111645 · GZJ | 510(k) clearances |
| Jan 7, 2010 | INF 4160 PLUS, MODEL D-FJ31FK092780 · LIH | 510(k) clearances |
| Dec 13, 2007 | FD EMS, MODEL # D-FJ30EK063642 · IPF | 510(k) clearances |
| Jan 25, 2006 | FD TENS 2030, MODEL DFJ24TK052813 · GZJ | 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
