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 Can-Am Surgical Corp. with 6 510(k) clearances. The most recent is a 510(k) clearance dated Apr 16, 1987: DISPOSABLE SYRINGE TUBERCULIN W/NEEDLE.
| Apr 16, 1987 | DISPOSABLE SYRINGE TUBERCULIN W/NEEDLEK870192 · FMF | 510(k) clearances |
| Apr 16, 1987 | DISPOSABLE SYRINGE W/O NEEDLEK870190 · FMF | 510(k) clearances |
| Apr 16, 1987 | DISPOSABLE SYRINGE WITH NEEDLEK870191 · FMF | 510(k) clearances |
| Feb 27, 1987 | A+MED DISPOSABLE NEEDLEK870193 · FMI | 510(k) clearances |
| Feb 4, 1987 | E-Z JECT INSULIN SYRINGEK870018 · FMF | 510(k) clearances |
| Jan 21, 1987 | AMG + MED LANCETK870017 · FMK | 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
