FDA 510(k) Applications Submitted by Vilex in Tennessee, Inc.
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K141937 | 07/17/2014 | TRIDENT FUSION IMPLANT | VILEX IN TENNESSEE, INC. |
| K150211 | 01/30/2015 | EzFuze Implant System | VILEX IN TENNESSEE, INC. |
| K190543 | 03/04/2019 | Cannulated Hemi Implant | Vilex in Tennessee, Inc. |
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