FDA 510(k) Applications Submitted by Ivory Super Holdco Inc. / Zest Anchors LLC
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K203701 | 12/18/2020 | Locator Overdenture Implant System | Ivory Super Holdco Inc. / Zest Anchors LLC |
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