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Orthalign, Inc. FDA Approvals
0 new drug approvals and 3 device clearances on file. This applicant is not matched to a listed company.
Newest first
A new drug approval is an original application; a 510(k) is a device shown equivalent to one already sold.
| Product |
|---|
| Lantern Knee Navigation Unit (406000-03);Lantern Hip Navigation Unit (502000-03)510(k)Jul 31, 2026Neurology |
| Packaged Assembly, Reusable Navigation Unit; Lantern ASC, Smart Pack kit, Knee510(k)Jun 2, 2026Neurology |
| Lantern® Hip510(k)Oct 3, 2024Neurology |