The following data is part of a premarket notification filed by Voco Gmbh with the FDA for Rebilda Sc.
| Device ID | K014111 |
| 510k Number | K014111 |
| Device Name: | REBILDA SC |
| Classification | Material, Tooth Shade, Resin |
| Applicant | VOCO GMBH 7527 WESTMORELAND AVE. St. Louis, MO 63105 |
| Contact | Evan Dick |
| Correspondent | Evan Dick VOCO GMBH 7527 WESTMORELAND AVE. St. Louis, MO 63105 |
| Product Code | EBF |
| CFR Regulation Number | 872.3690 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2001-12-14 |
| Decision Date | 2002-03-06 |
| Summary: | summary |