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 Neuro Technology with 5 510(k) clearances. The most recent is a 510(k) clearance dated Apr 19, 1993: E-SP COMBINED EPI SPINAL MINISET.
| Apr 19, 1993 | E-SP COMBINED EPI SPINAL MINISETK925014 · CAZ | 510(k) clearances |
| May 30, 1991 | MICRO-SP LUMBAR PUNCTURE (SPINAL) NEEDLEK901810 · BSP | 510(k) clearances |
| May 28, 1991 | ADD'L DATA E-SP MULTIPURPOSE EPIDURAL SPINALNEEDLEK901811 · BSP | 510(k) clearances |
| Sep 13, 1982 | STIMPENK822139 · BXN | 510(k) clearances |
| Jul 30, 1982 | NEUROSTIM IIK822138 · BXN | 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
