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 Confirma, Inc. with 9 510(k) clearances. The most recent is a 510(k) clearance dated Nov 6, 2009: CADSTREAM VERSION 5.
| Date | Record | Source |
|---|---|---|
| Nov 6, 2009 | CADSTREAM VERSION 5K092954 · LLZ | 510(k) clearances |
| Feb 2, 2009 | CADSTREAM, VERSION 5.0K081556 · LLZ | 510(k) clearances |
| Jul 9, 2007 | CONFIRMA BREAST MRI INTERVENTIONAL COMPONENTSK071534 · MOS | 510(k) clearances |
| Mar 29, 2006 | ACCESS BREAST COIL 4/SMSK060547 · MOS | 510(k) clearances |
| Aug 24, 2005 | ACCESS BREAST COILK052045 · MOS | 510(k) clearances |
| Jan 6, 2005 | CADSTREAM VERSION 4.0K043216 · LLZ | 510(k) clearances |
| Jul 7, 2004 | CADSTREAM VERSION 3.1K041020 · LNH | 510(k) clearances |
| Aug 6, 2003 | CADSTREAMK031779 · LLZ | 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
