FDA 510(k) Applications Submitted by David Kim
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K170421 | 02/13/2017 | ET Hybrid Abutment | Hiossen Inc. |
| K180527 | 02/28/2018 | IS3 | Hiossen, Inc. |
| K151542 | 06/08/2015 | A-Oss | HIOSSEN INC. |
| K151626 | 06/17/2015 | ET III Bio-SA Fixture System | HiOSSEN Inc. |
| K162390 | 08/26/2016 | ET Hybrid Abutment | HIOSSEN INC. |
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