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 13, 2026, FDA's public records list Biosurge with 5 510(k) clearances. The most recent is a 510(k) clearance dated Nov 21, 1988: ASD SINGLE LUMEN NEEDLE.
| Date | Record | Source |
|---|---|---|
| Nov 21, 1988 | ASD SINGLE LUMEN NEEDLEK884620 · FMI | 510(k) clearances |
| Feb 29, 1988 | BIOSURGE MODEL ILVC-1K875016 · DWS | 510(k) clearances |
| Feb 19, 1988 | ASD-BIO ANTI-STICK DEVICEK874602 · FMI | 510(k) clearances |
| Feb 12, 1988 | BIOSURGE MODEL OASYS-IIK875023 · CAC | 510(k) clearances |
| May 21, 1987 | BIOSURGE MODEL OASYSK871258 · CAC | 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
