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 Glenroe Technologies with 9 510(k) clearances. The most recent is a 510(k) clearance dated Feb 24, 1998: GLENROE CHAIN.
| Date | Record | Source |
|---|---|---|
| Feb 24, 1998 | GLENROE CHAINK980053 · ECI | 510(k) clearances |
| Jan 27, 1995 | GLENROE ORTHO-SILK945535 · EGD | 510(k) clearances |
| Jan 6, 1994 | GLENROE ELASTIBITE STIMULATORK924351 · KMY | 510(k) clearances |
| Aug 24, 1993 | GLENROE PLASTIC BRACKETK932920 · DYW | 510(k) clearances |
| Jul 22, 1993 | GLENROE CHAINK931462 · ECI | 510(k) clearances |
| Apr 27, 1993 | TUFF TIESK924140 · ECI | 510(k) clearances |
| Apr 8, 1993 | GLENROE ORTHO SEPSK924139 · ECI | 510(k) clearances |
| Mar 31, 1993 | EJECTORK924211 · DYN | 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
