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 RLN Systems, Inc. with 5 510(k) clearances. The most recent is a 510(k) clearance dated Jan 16, 2001: LARYNGEAL SURFACE ELECTRODE-ENDOTRACHEAL TUBE, M-500-ET, LSE-ET.
| Date | Record | Source |
|---|---|---|
| Jan 16, 2001 | LARYNGEAL SURFACE ELECTRODE-ENDOTRACHEAL TUBE, M-500-ET, LSE-ETK003745 · ETN | 510(k) clearances |
| Dec 22, 1995 | NERVE LOCATOR/MONITOR SYSTEM MODIFICATIONK954601 · ETN | 510(k) clearances |
| Nov 24, 1992 | RLN NERVE LOCATOR/MONITOR; MODEL AK925008 · ETN | 510(k) clearances |
| Sep 30, 1992 | NERVE LOCATOR/MONITOR SYSTEM, MODIFICATIONK912508 · ETN | 510(k) clearances |
| Dec 8, 1989 | HEMOSTAT/STIMULATOR PROBEK895676 · ETN | 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
