The following data is part of a premarket notification filed by Dentis Co. Ltd. with the FDA for Modificaton To: Dentis Dental Implant System.
| Device ID | K082843 |
| 510k Number | K082843 |
| Device Name: | MODIFICATON TO: DENTIS DENTAL IMPLANT SYSTEM |
| Classification | Implant, Endosseous, Root-form |
| Applicant | DENTIS CO. LTD. 13340 E FIRESTONE BLVD SUITE J Santa Fe Springs, CA 90670 |
| Contact | Jung Bae Bang |
| Correspondent | Jung Bae Bang DENTIS CO. LTD. 13340 E FIRESTONE BLVD SUITE J Santa Fe Springs, CA 90670 |
| Product Code | DZE |
| CFR Regulation Number | 872.3640 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2008-09-29 |
| Decision Date | 2009-06-19 |
| Summary: | summary |