The following data is part of a premarket notification filed by Metalor Dental Usa Corp. with the FDA for Endo-core.
| Device ID | K912720 |
| 510k Number | K912720 |
| Device Name: | ENDO-CORE |
| Classification | Post, Root Canal |
| Applicant | METALOR DENTAL USA CORP. 457 LAUREL RD. BOX 369 Rockville Centre, NY 11571 -0369 |
| Contact | Brian F Schiller |
| Correspondent | Brian F Schiller METALOR DENTAL USA CORP. 457 LAUREL RD. BOX 369 Rockville Centre, NY 11571 -0369 |
| Product Code | ELR |
| CFR Regulation Number | 872.3810 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1991-06-18 |
| Decision Date | 1991-08-20 |