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 14, 2026, FDA's public records list Neuromed with 15 510(k) clearances. The most recent is a 510(k) clearance dated May 22, 1996: ONE STEP CONNECT LEADS (QUATTRODE, OCTRODE, CERVITRODE).
| May 22, 1996 | ONE STEP CONNECT LEADS (QUATTRODE, OCTRODE, CERVITRODE)K960728 · GZB | 510(k) clearances |
| Dec 15, 1994 | NEUROMED OCTRODE MODEL MNR-88A-B-C NEUROSTIM RECK930536 · GZB | 510(k) clearances |
| Dec 12, 1994 | NEUROMED OCTRODE MODEL MNT-98 NEUROSTIMULATOR TRANK930498 · GZB | 510(k) clearances |
| Feb 2, 1994 | INTRODE INT-8K930242 · GZB | 510(k) clearances |
| May 5, 1993 | NEUROMED MODEL OCA-30 OCTODE AND MODEL SCA-30K921319 · GZB | 510(k) clearances |
| Mar 11, 1991 | NEUROMED OCTRODE MODEL MNR-88B/88C NEUROSTIM SYSTK905596 · GZB | 510(k) clearances |
| Jan 25, 1991 | NEUROMED MODEL 1992 LS LAMITRODE LEADK905255 · GZB | 510(k) clearances |
| Jan 16, 1991 | NEUROMED TS8 TEST STIMULATORK903814 · GZB | 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
