Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field.. FDA files no records under this name; these are its 3 companies' records, each linked to the record.
As of Nov 14, 2026, FDA's public records list Weigao Group and its 3 subsidiaries with 8 510(k) clearances. The most recent is a 510(k) clearance dated Aug 4, 2017: Premier.
Drug approvals, 510(k) clearances, recalls and letters, 2017 to 2026 to date, Weigao Group and its 3 subsidiaries
A hatched bar is a year that is not over, so its count covers only part of the year.
| Aug 4, 2017 | PremierK170861 · NKB | 510(k) clearances |
| Apr 1, 2016 | PremierK160320 · MNI | 510(k) clearances |
| Jul 15, 2014 | MILESTONE SPINAL SYSTEMK133053 · MAX | 510(k) clearances |
| Apr 12, 2013 | INTRAMEDULLARY NAIL SYSTEMK122994 · MNH | 510(k) clearances |
| Apr 5, 2013 | LOCKING BONE PLATES AND SCREWSK130340 · HRS | 510(k) clearances |
| Feb 1, 2013 | ANTERIOR CERVICAL PLATE SYSTEMK123578 · KWQ | 510(k) clearances |
| Oct 24, 2012 | INTRAMEDULLARY NAIL SYSTEMK121312 · HSB | 510(k) clearances |
| Mar 23, 2009 | DISPOSABLE ANGIOGRAPHIC SYRINGE, MODEL(S) CT-200-NE, CT-200-MA, CT-200+200-MA, CT-200-LF, CT -100-NE, CT-200NE, CT-50+CTK082439 · DXT | 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
