Pharmaceutical companyLabelled 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 SanofiLabelled 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 Sanofi group view.
As of Nov 15, 2026, FDA's public records list Sterling Drug with 9 510(k) clearances. The most recent is a 510(k) clearance dated Jun 5, 1990: GREEN LABEL BIOBRANE II AND RED LABEL BIOBRANE II.
| Jun 5, 1990 | GREEN LABEL BIOBRANE II AND RED LABEL BIOBRANE IIK901369 · KGN | 510(k) clearances |
| Nov 28, 1989 | BIOBRANE(R) IIK896110 · KGN | 510(k) clearances |
| Jan 27, 1988 | WINTHROP PHARMACEUTICALS CONTRAST MEDIA WARMERK875275 · JTQ | 510(k) clearances |
| Apr 5, 1984 | PERIOGRAF DURAPATITE 40-60 MESHK840260 · LYC | 510(k) clearances |
| Feb 24, 1982 | CONAGRAF TM DURAPATITE CONESK820023 · LYC | 510(k) clearances |
| Feb 24, 1982 | EMPTY STERILE CARPUJECTK820164 · FMF | 510(k) clearances |
| Jan 5, 1982 | ALVEOGRAF DURAPATITE(18-40 MESH)K813257 · DZE | 510(k) clearances |
| Nov 20, 1981 | PERIOGRAFK813070 · LYC | 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
