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 Moe with 6 510(k) clearances. The most recent is a 510(k) clearance dated Mar 23, 1989: BIOFEEDBACK DEVICE ACCESS. PI1,2,3,4,5/LIGHT BAR.
| Date | Record | Source |
|---|---|---|
| Mar 23, 1989 | BIOFEEDBACK DEVICE ACCESS. PI1,2,3,4,5/LIGHT BARK884849 · HCC | 510(k) clearances |
| Feb 3, 1989 | BIOFEEDBACK DEVICE TG3, TG4K884851 · HCC | 510(k) clearances |
| Feb 2, 1989 | BASIC BIOFEEDBACK,TMG4.1, SA1/2, EEG4/5, IR RECEIVK884848 · HCC | 510(k) clearances |
| Feb 2, 1989 | BIOFEEDBACK EEG1/2, EEG ULTRA LOW NOISE, SYC1K884853 · HCC | 510(k) clearances |
| Feb 2, 1989 | BIOFEEDBACK DEVICE EMG1, EMG ULTRA LOW NOISE OPTI.K884852 · HCC | 510(k) clearances |
| Feb 2, 1989 | BIOFEEDBACK TMG1, 4, BIO1, PA1, 2, BA1/BA30K884850 · HCC | 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
