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COMPANY

MiRus

HQ: Marietta, GA source · mirusmed.com ↗ · Southeast

FDA-cleared device company

Location: Marietta, GA · source · Oct 15, 2026

Profile checked Oct 10, 2026

3FDA records (2 yrs)

Timeline

  1. FDA FDA 510(k) clearance: EUROPA™ Posterior Cervical Fusion Navigated Instruments — K253444, Mar 18, 2026. Applicant at approval: MiRus, LLC. source ↗
  2. FDA FDA 510(k) clearance: ATLAS™ Expandable Osteotomy Wedge System — K252733, Feb 19, 2026. Applicant at approval: MiRus, LLC. source ↗
  3. FDA FDA 510(k) clearance: EUROPA™ Posterior Cervical Fusion System — K242516, Nov 19, 2024. Applicant at approval: MiRus, LLC. source ↗

FDA records (last 2 years)

Connect

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

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