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.. FDA records under its name, each linked to the record.
As of Nov 13, 2026, FDA's public records list Sterngold with 12 510(k) clearances. The most recent is a 510(k) clearance dated Nov 10, 2009: STERNGOLD 2.2MM ANGLES MICRO ERA DENTAL IMPLANT SYSTEM.
| Date | Record | Source |
|---|---|---|
| Nov 10, 2009 | STERNGOLD 2.2MM ANGLES MICRO ERA DENTAL IMPLANT SYSTEMK092434 · DZE | 510(k) clearances |
| Oct 28, 2004 | STERNGOLD 3.25 ERA DENTAL IMPLANT SYSTEMK041271 · DZE | 510(k) clearances |
| Jan 17, 2003 | STERNGOLD ACID ETCH DENTAL IMPLANT SYSTEMK023580 · DZE | 510(k) clearances |
| Sep 19, 2002 | STERNGOLD 1, MODEL 1127781K022252 · EJS | 510(k) clearances |
| Jun 26, 2002 | CRITERTION, MODEL #1067511K021741 · EJT | 510(k) clearances |
| Jun 26, 2002 | ERA IMPLANTK021045 · DZE | 510(k) clearances |
| May 16, 2002 | STERNGOLD 66, MODEL #1180230K021367 · EJS | 510(k) clearances |
| Apr 4, 2002 | APOLLO, MODEL 1124525K020949 · EJT | 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
