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 Dana Products, Inc. with 9 510(k) clearances. The most recent is a 510(k) clearance dated Feb 11, 2014: DANA REUSABLE TEST PACK.
| Feb 11, 2014 | DANA REUSABLE TEST PACKK133267 · FRC | 510(k) clearances |
| Nov 25, 2013 | DANA REUSABLE BI TEST PACKK130135 · JOJ | 510(k) clearances |
| Feb 27, 2013 | DANA REUSABLE BOWIE TEST PACK FOR DANA BOWIE DICK INDICATORSK120592 · JOJ | 510(k) clearances |
| Apr 29, 2011 | REUSABLE TEST PACK FOR DANA EMULATING INDICATORSK110253 · JOJ | 510(k) clearances |
| Feb 16, 2011 | DANA REUSABLE TESTPACK FOR STEAM STERILIZATION FOR 10 MINUTE EXTENDED CYCLESK103321 · FRC | 510(k) clearances |
| Jan 13, 2011 | DANA EMULATING INDICATORK100891 · JOJ | 510(k) clearances |
| Dec 20, 2010 | DANA REUSABLE TEST PACK FOR STEAM STERILIZATIONK102761 · JOJ | 510(k) clearances |
| Mar 18, 2010 | DANA REUSABLE TEST PACK FOR STEAM STERILIZATIONK092944 · FRC | 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
