FDA 510(k) Applications Submitted by ANAXDENT GMBH
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K023079 | 09/16/2002 | NEW OUTLINE | ANAXDENT GMBH |
| K112044 | 07/18/2011 | ANAXBLEND MODEL 20XXX (SEVERAL), ANAXGUM MODEL 25XXX (U), MOCK-UP DIRECT MODEL 240XXX (U), MOCK-UP DIRECT FLOW MODEL 24A | ANAXDENT GMBH |
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