FDA 510(k) Applications Submitted by ROBERT A SILVERMAN
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K070215 | 01/23/2007 | TOKUYAMA BOND FORCE | TOKUYAMA DENTAL CORPORATION |
| K071190 | 04/30/2007 | ROOT ZX II | J. MORITA USA, INC. |
| K063529 | 11/22/2006 | PENCURE, MODEL VL-7 | J. MORITA USA, INC. |
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