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 its name, each linked to the record.
As of Nov 13, 2026, FDA's public records list Orthopro with 7 510(k) clearances. The most recent is a 510(k) clearance dated Feb 28, 2013: ANKLE TRAUMA SYSTEM.
| Feb 28, 2013 | ANKLE TRAUMA SYSTEMK122936 · HRS | 510(k) clearances |
| May 25, 2012 | I-FUSE HAMMER TOE SYSTEMSK113006 · HWC | 510(k) clearances |
| Nov 22, 2010 | CSTS SCREWK093055 · HWC | 510(k) clearances |
| Feb 29, 2008 | DC ULNAR SHORTENING SYSTEMK073228 · HRS | 510(k) clearances |
| Jul 13, 2007 | ORTHOPRO STEINMAN PINS AND KIRSCHNER WIRESK070555 · HTY | 510(k) clearances |
| May 23, 2007 | METAL HEMI IMPLANTK071243 · KWD | 510(k) clearances |
| Nov 13, 2006 | ORTHROPRO HEMI TOEK062908 · KWD | 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
