This page includes the latest FDA filings for Koning Corp. Currently, you will find the latest 100 filings for Premarket Notifications, Premarket Applications, De Novo Applications, and GUDID registrations.
| Registration Number | 3008513054 |
| FEI Number | 3008513054 |
| Name | KONING CORPORATION |
| Owner & Operator | Koning Corporation |
| Contact Address | 150 Lucius Gordon Drive Suite 112 West Henrietta NY 14586 US |
| Registration Status | 1 |
| Initial Importer | N |
| Registration Expiration | 2020-04-25 |
| Registration Address | 555 Oakbrook Parkway, Suite 640 Norcross, GA 30093 US |
| Establishment Type | Complaint File Establishment per 21 CFR 820.198 |
Device Company | Device | Date |
|---|---|---|
| KONING CORPORATION | Koning Breast CT System CBCT 1000 | 2025-07-25 |
| KONING CORPORATION | Koning Breast CT, KBCT | 2017-10-24 |
| KONING CORPORATION | KONING BREAST CT (MODEL CBCT 1000) | 2016-10-06 |
KONING CORPORATION | KBCT | 2016-01-22 |
| KONING CORPORATION | KONING BREAST CT (MODEL CBCT1000) | 2015-01-14 |
| NCAGE Code | 0JLM6 | KONING CORP |
| NCAGE Code | 49ZB4 | KONING CORPORATION |
| CAGE Code | 0JLM6 | KONING CORP |
| CAGE Code | 49ZB4 | KONING CORPORATION |
| S.A.M. Registration | 49ZB4 [145060716] | KONING CORPORATION |
| SEC | 0001174199 | KONING CORP |