Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field. in United StatesLabelled 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 Kinamed with 35 510(k) clearances. The most recent is a 510(k) clearance dated Aug 1, 2018: SuperCable® Iso-Elastic™ Cerclage System.
Drug approvals, 510(k) clearances, recalls and letters, 2017 to 2026 to date
A hatched bar is a year that is not over, so its count covers only part of the year.
| Date | Record | Source |
|---|---|---|
| Aug 1, 2018 | SuperCable® Iso-Elastic™ Cerclage SystemK181749 · JDQ | 510(k) clearances |
| Apr 5, 2013 | NEUROPRO LOW PROFILE CRANIAL PLATING SYSTEMK122049 · GWO | 510(k) clearances |
| Jan 12, 2011 | ISO-ELASTIC CERCLAGE SYSTEM (1MM AND 2MM CABLE DIAMETER)K102834 · JDQ | 510(k) clearances |
| Nov 9, 2007 | SUPERCABLE GRIP AND PLATE SYSTEMK072250 · KTT | 510(k) clearances |
| May 24, 2005 | NAVIPRO SHOULDER SOFTWARE MODULEK050897 · HAW | 510(k) clearances |
| Mar 11, 2004 | NAVIPRO KNEE SOFTWARE MODULEK033668 · HAW | 510(k) clearances |
| Dec 19, 2003 | GEM INSET PATELLAR COMPONENTK032950 · JWH | 510(k) clearances |
| Oct 21, 2003 | ISO-ELASTIC CERCLAGE SYSTEMK030256 · JDQ | 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
