FDA 510(k) Applications Submitted by OrthAlign, Inc
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K130387 | 02/15/2013 | ORTHOALIGN PLUS SYSTEM | ORTHALIGN, INC |
| K091411 | 05/13/2009 | KNEEALIGN SYSTEM | ORTHALIGN, INC |
| K093998 | 12/28/2009 | KNEEALIGN SYSTEM WITH REFERENCE SENSOR | ORTHALIGN, INC |
| K103829 | 12/30/2010 | KNEEALIGN SYSTEM | ORTHALIGN, INC |
| K140331 | 02/10/2014 | ORTHALIGN PLUS SYSTEM | ORTHALIGN, INC |
| K242616 | 09/03/2024 | Lantern« Hip | OrthAlign, Inc |
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