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 14, 2026, FDA's public records list Spirus Medical with 5 510(k) clearances. The most recent is a 510(k) clearance dated May 6, 2008: SPIRUS MEDICAL ENDO-EASE ENDOSCOPIC OVERTUBE.
| May 6, 2008 | SPIRUS MEDICAL ENDO-EASE ENDOSCOPIC OVERTUBEK080050 · FED | 510(k) clearances |
| Apr 3, 2008 | SPIRUS MEDICAL SURGICAL INSTRUMENTK080042 · KMJ | 510(k) clearances |
| Oct 13, 2006 | MODIFICATION TO ENDO-EASEK062805 · FED | 510(k) clearances |
| Aug 4, 2006 | ENDO-EASE ENDOSCOPIC OVERTUBEK060235 · FDA | 510(k) clearances |
| Sep 14, 2005 | ENDO-EASE ENDOSCOPIC OVERTUBEK052084 · FED | 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
