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 Frontier Medical Devices with 5 510(k) clearances. The most recent is a 510(k) clearance dated Jan 13, 2016: Frontier Medical Devices In-Line Orthopedic Cable Cerclage System.
| Jan 13, 2016 | Frontier Medical Devices In-Line Orthopedic Cable Cerclage SystemK153242 · JDQ | 510(k) clearances |
| Oct 30, 2015 | Frontier Medical Devices In-line Orthopedic Cable Cerclage SystemK151888 · JDQ | 510(k) clearances |
| Aug 20, 2015 | Frontier Medical Devices Posterior Cable Screw SystemK151346 · JDQ | 510(k) clearances |
| Feb 26, 2015 | Ancora LLC Interbody Fusion DeviceK143228 · OVD | 510(k) clearances |
| Nov 1, 2012 | FRONTIER SADL INTERBODY FUSION DEVICEK112700 · OVD | 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
