Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field.. FDA records under 3 spellings of its name, each linked to the record.
As of Nov 14, 2026, FDA's public records list Ortho Solutions with 6 510(k) clearances and 4 device recalls. The most recent is a device recall dated Oct 10, 2017: SYSTEM 26. Part Numbers: OS900035-NS; OS900036-NS; OS900037-NS; OS900038-NS; OS9000….
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.
| Oct 10, 2017 | SYSTEM 26. Part Numbers: OS900035-NS; OS900036-NS; OS900037-NS; OS900038-NS; OS900040-NS; OS900041-NS; OS900042-NS; OS900043-NS; OSClass II · Following the identification of corrosion residue found inside the cannulated devices in Forefoot and Midfoot trays Orh | Device recalls |
| Jul 23, 2014 | ORTHO SOLUTIONS ULTOS PLATING SYSTEMK141784 · HRS | 510(k) clearances |
| Sep 14, 2012 | OXFORD ANKLE FUSION NAIL(AFN) SYSTEMK121575 · HSB | 510(k) clearances |
| May 29, 2012 | ORTHO SOLUTIONS TRAUMA PLATES FOR OSTEOSYSNTHESISK120360 · HRS | 510(k) clearances |
| Feb 7, 2012 | ORTHO SOLUTIONS EXTREMITY FIXATION IMPLANTS FOR OSTEOSYSNTHESISK111678 · HRS | 510(k) clearances |
| Dec 19, 2011 | ORTHO SOLUTIONS TRAUMA IMPLANTS FOR OSTEOSYNTHESISK110895 · HWC | 510(k) clearances |
| Jan 20, 2011 | ORTHO SOLUTIONS - STERILE, DRILLS, TAPS, GUIDE PINS & WIRESK102743 · HWE | 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
