FirmLabelled 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 15, 2026, FDA's public records list Alliance Partners with 10 510(k) clearances and 1 device recall. The most recent is a 510(k) clearance dated Aug 6, 2020: Medina Anterior Cervical Plate 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.
| Aug 6, 2020 | Medina Anterior Cervical Plate SystemK201521 · KWQ | 510(k) clearances |
| Mar 22, 2018 | Alamo® CK173128 · ODP | 510(k) clearances |
| Jun 9, 2015 | Nakoma-SL Anterior Cervical Plating System's Variable Single Barrel Drill Guide Product Usage: The Nakoma-SL ACP System is intended for Class II · Inadequate interference between the screw and the plate when screw implanted into the plate at angulation greater than 7 | Device recalls |
| Feb 27, 2015 | ALLIANCE SPINE RAAS CRANIAL PLATING SYSTEMK141123 · GWO | 510(k) clearances |
| Nov 6, 2014 | NAKOMA ACPK141993 · KWQ | 510(k) clearances |
| Apr 21, 2014 | ALAMO TK140303 · MAX | 510(k) clearances |
| Jan 9, 2014 | ALAMO CK133321 · ODP | 510(k) clearances |
| Oct 5, 2012 | ALAMO TK120401 · MAX | 510(k) clearances |
| Sep 4, 2012 | ALAMO PK122047 · MAX | 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
