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 15, 2026, FDA's public records list Altatec Biotechnologies and its 1 subsidiaries with 5 510(k) clearances. The most recent is a 510(k) clearance dated Aug 22, 2003: ALTATEC CERAMIC ABUTMENT.
| Aug 22, 2003 | ALTATEC CERAMIC ABUTMENTK032448 · NHA | 510(k) clearances |
| Aug 14, 2002 | SCREWLINEK022425 · DZE | 510(k) clearances |
| Jan 28, 2000 | CAMLOG ROOTFORM IMPLANT SYSTEMK000100 · DZE | 510(k) clearances |
| Jan 28, 2000 | CAMLOG SCREW IMPLANT SYSTEMK000099 · DZE | 510(k) clearances |
| Jan 28, 2000 | CAMLOG CYLINDER IMPLANT SYSTEMK000065 · DZE | 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
