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 Acme-Monaco Corp. with 5 510(k) clearances. The most recent is a 510(k) clearance dated Jul 20, 2012: SLIDEWIRETM(TRADEMARK PENDING).
| Jul 20, 2012 | SLIDEWIRETM(TRADEMARK PENDING)K113162 · DQX | 510(k) clearances |
| Aug 19, 1992 | GUIDEWIRES, VARIOUS TYPESK920884 · DQX | 510(k) clearances |
| Apr 9, 1990 | ACME PREFORMED COATED LIGATURE TIES (TOOTH SHADE)K895854 · EJF | 510(k) clearances |
| Jan 29, 1990 | ACME COATED ORTHODONTIC ARCHWIREK895483 · EJF | 510(k) clearances |
| Nov 18, 1988 | ACME GUIDEWIRES FOR PERCUTANEOUS INSERTION OF CATHK883763 · KOD | 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
