FDA FDA 510(k) clearance: Lantern Knee Navigation Unit (406000-03);Lantern Hip Navigation Unit (502000-03) — K262253, Jul 31, 2026. Applicant at approval: Orthalign, Inc. source ↗
FDA FDA 510(k) clearance: Packaged Assembly, Reusable Navigation Unit; Lantern ASC, Smart Pack kit, Knee — K253507, Jun 2, 2026. Applicant at approval: Orthalign, Inc. source ↗
FDA records (last 2 years)
FDA 510(k) clearance: Lantern Knee Navigation Unit (406000-03);Lantern Hip Navigation Unit (502000-03) — K262253, Jul 31, 2026. Applicant at approval: Orthalign, Inc. source ↗
FDA 510(k) clearance: Packaged Assembly, Reusable Navigation Unit; Lantern ASC, Smart Pack kit, Knee — K253507, Jun 2, 2026. Applicant at approval: Orthalign, Inc. source ↗
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