The following data is part of a premarket notification filed by Angelus Industria De Productos Odontologicos with the FDA for Interlig.
| Device ID | K123823 |
| 510k Number | K123823 |
| Device Name: | INTERLIG |
| Classification | Material, Tooth Shade, Resin |
| Applicant | ANGELUS INDUSTRIA DE PRODUCTOS ODONTOLOGICOS 18851 NE 29TH AVE 720 Aventura, FL 33180 |
| Contact | Lilian Llull |
| Correspondent | Lilian Llull ANGELUS INDUSTRIA DE PRODUCTOS ODONTOLOGICOS 18851 NE 29TH AVE 720 Aventura, FL 33180 |
| Product Code | EBF |
| CFR Regulation Number | 872.3690 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2012-12-12 |
| Decision Date | 2013-05-31 |
| Summary: | summary |