FDA 510(k) Applications Submitted by REMEDENT NV
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K023652 | 10/30/2002 | REMECURE MODEL CL 15E | REMEDENT NV |
| K082594 | 09/08/2008 | REMESENSE | REMEDENT NV |
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