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COMPANY

Ortho Development

HQ: Draper, UT source · odev.com ↗

FDA-cleared device company

Location: Draper, UT · source · Oct 15, 2026

Profile checked Oct 10, 2026

4FDA records (2 yrs)

Timeline

  1. FDA FDA 510(k) clearance: Balanced Knee System TriMax Porous Femoral Components — K253161, Dec 19, 2025. Applicant at approval: Ortho Development Corp. source ↗
  2. FDA FDA 510(k) clearance: Trivicta® Hip Stem — K251052, May 22, 2025. Applicant at approval: Ortho Development Corp. source ↗
  3. FDA FDA 510(k) clearance: BKS Revision System — K242984, Oct 25, 2024. Applicant at approval: Ortho Development Corp. source ↗
  4. FDA FDA 510(k) clearance: Legend® Acetabular Shell — K242833, Oct 11, 2024. Applicant at approval: Ortho Development Corp. source ↗

FDA records (last 2 years)

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LinkedIn page linked from the company's own site: source · seen 2026-10-12

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