MAGICFIL
Material, Tooth Shade, Resin
DMG USA, INC.
The following data is part of a premarket notification filed by Dmg Usa, Inc. with the FDA for Magicfil.
Pre-market Notification Details
| Device ID | K013571 |
| 510k Number | K013571 |
| Device Name: | MAGICFIL |
| Classification | Material, Tooth Shade, Resin |
| Applicant | DMG USA, INC. 5 WHITCOMB AVE. Ayer, MA 01432 |
| Contact | Pamela Papineau |
| Correspondent | Pamela Papineau DMG USA, INC. 5 WHITCOMB AVE. Ayer, MA 01432 |
| Product Code | EBF |
| CFR Regulation Number | 872.3690 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Abbreviated |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2001-10-29 |
| Decision Date | 2002-01-17 |
| Summary: | summary |
Trademark Results [MAGICFIL]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 MAGICFIL 76241333 2735319 Dead/Cancelled |
ERNST MUHLBAUER GMBH & CO, KG 2001-04-16 |
© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.