FDA 510(k) Applications Submitted by exocad GmbH
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K193352 | 12/04/2019 | AbutmentCAD | exocad GmbH |
| K183458 | 12/13/2018 | exoplan 2.3 | exocad GmbH |
| K213302 | 10/04/2021 | exoplan | exocad GmbH |
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