The following data is part of a premarket notification filed by Dio Corporation with the FDA for Uf(ii) Narrow Implant System - Fixture, Uf(ii) Narrow Implant System - Suprastructure.
Device ID | K161987 |
510k Number | K161987 |
Device Name: | UF(II) Narrow Implant System - Fixture, UF(II) Narrow Implant System - Suprastructure |
Classification | Implant, Endosseous, Root-form |
Applicant | DIO CORPORATION 66, CENTUM SEO-RO Busan, KR 48058 |
Contact | Sangin Park |
Correspondent | Peter Kang DIO USA 3470 WILSHIRE BLVD. #620 Los Angeles, CA 90010 |
Product Code | DZE |
CFR Regulation Number | 872.3640 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2016-07-19 |
Decision Date | 2017-02-21 |