The following data is part of a premarket notification filed by Cowellmedi Co., Ltd with the FDA for Inno Sla Submerged Implant System.
| Device ID | K132242 |
| 510k Number | K132242 |
| Device Name: | INNO SLA SUBMERGED IMPLANT SYSTEM |
| Classification | Implant, Endosseous, Root-form |
| Applicant | COWELLMEDI CO., LTD 325 N. PUENTE ST UNIT B Brea, CA 92821 |
| Contact | Susan Park |
| Correspondent | Susan Park COWELLMEDI CO., LTD 325 N. PUENTE ST UNIT B Brea, CA 92821 |
| Product Code | DZE |
| CFR Regulation Number | 872.3640 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2013-07-18 |
| Decision Date | 2013-12-06 |
| Summary: | summary |