FDA 510(k) Applications Submitted by DENTSPLY GENDEX
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K032355 | 07/30/2003 | ORTHORALIX 9200 DDE, ORTHORALIX 9200 DDE PLUS CEPH, MODELS 5105 0161WW, 5105 0181WW | DENTSPLY GENDEX |
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