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restor3d

HQ: Durham, NC source · restor3d.com ↗

FDA-cleared device company

Location: Durham, NC · source · Oct 14, 2026

Profile checked Oct 10, 2026

8FDA records (2 yrs)

Timeline

  1. FDA FDA 510(k) clearance: Veritas Shoulder System — K260556, Jul 1, 2026. Applicant at approval: Restor3D. source ↗
  2. FDA FDA 510(k) clearance: Veritas Reverse Total Shoulder System — K253992, May 7, 2026. Applicant at approval: Restor3D. source ↗
  3. FDA FDA 510(k) clearance: Velora Acetabular System — K252067, Dec 5, 2025. Applicant at approval: Restor3D, Inc. source ↗
  4. FDA FDA 510(k) clearance: Kinos Total Ankle System — K252454, Sep 3, 2025. Applicant at approval: Restor3D. source ↗
  5. FDA FDA 510(k) clearance: restor3d Reverse Total Shoulder Arthroplasty System — K243643, May 19, 2025. Applicant at approval: Restor3D. source ↗
  6. FDA FDA 510(k) clearance: iTotal® Identity™ Cruciate Retaining 3DP Porous Knee Replacement System — K243768, Mar 27, 2025. Applicant at approval: Restor3D, Inc. source ↗
  7. FDA FDA 510(k) clearance: TIDAL Fusion Cage System — K242356, Mar 24, 2025. Applicant at approval: Restor3D, Inc. source ↗
  8. FDA FDA 510(k) clearance: Kinos Total Ankle System — K242868, Oct 18, 2024. Applicant at approval: Restor3D. source ↗

FDA records (last 2 years)

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