Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field. in United StatesLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field., part of Johnson & JohnsonLabelled 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. See the Johnson & Johnson group view.
As of Nov 14, 2026, FDA's public records list Depuyacromed with 48 510(k) clearances. The most recent is a 510(k) clearance dated Apr 2, 2004: EAGLE ANTERIOR CERVIAL PLATE SYSTEM.
| Apr 2, 2004 | EAGLE ANTERIOR CERVIAL PLATE SYSTEMK040197 · KWQ | 510(k) clearances |
| Jun 23, 2003 | DEPUY ACROMED VBR SYSTEMK031635 · MQP | 510(k) clearances |
| Apr 10, 2003 | DEPUY ACROMED VBR SYSTEMK030833 · MQP | 510(k) clearances |
| Feb 26, 2003 | MODIFICATION TO MOSS MIAMI SPINAL SYSTEM POLYAXIAL SCREWSK030383 · MNH | 510(k) clearances |
| Feb 14, 2003 | SURGICAL TITANIUM MESH SYSTEMK030249 · MQP | 510(k) clearances |
| Feb 5, 2003 | SUMMIT OCT SPINAL SYSTEM MINIPOLYAXIAL SCREWSK030103 · MNI | 510(k) clearances |
| Jan 29, 2003 | DEVEX MESH SYSTEMK023835 · MQP | 510(k) clearances |
| Jan 28, 2003 | MONARCH SPINE SYSTEMK024348 · MNH | 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
