Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field.. FDA records under 2 spellings of its name, each linked to the record.
As of Nov 13, 2026, FDA's public records list Surgimed with 6 510(k) clearances. The most recent is a 510(k) clearance dated Feb 8, 2007: FORSURE DISPOSABLE SYRINGE WITH NEEDLE, MODEL 1CC, 3C, 5CC, 10CC, 20CC, 50CC.
| Feb 8, 2007 | FORSURE DISPOSABLE SYRINGE WITH NEEDLE, MODEL 1CC, 3C, 5CC, 10CC, 20CC, 50CCK062753 · FMF | 510(k) clearances |
| Apr 25, 1985 | SURGIMED - SURGICAL BLADESK851157 · GES | 510(k) clearances |
| Jul 13, 1984 | SILVERTORQUE CEREBRAL CATHETERK840762 · DQY | 510(k) clearances |
| Jun 13, 1984 | SILVERTORQUE CARDIAC CATHETERSK840763 · DQO | 510(k) clearances |
| Jun 11, 1984 | SILVERTORQUE VISCERAL CATHETERK840761 · DQY | 510(k) clearances |
| Jul 28, 1981 | BALLOON CATHETERK810689 · | 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
