This page includes the latest FDA filings for Kainos Laboratories Inc. Currently, you will find the latest 100 filings for Premarket Notifications, Premarket Applications, De Novo Applications, and GUDID registrations.
| JAPAN | TOKYO STOCK EXCHANGE | 4556 | DUNS 691688980 |
| Registration Number | 3008178161 |
| FEI Number | 3008178161 |
| Name | KAINOS LABORATORIES, INC., KASAMA FACTORY |
| Owner & Operator | KAINOS LABORATORIES INC |
| Contact Address | 38-18 Hongo 2-Chome Bunkyo-Ku Tokyo JP-13 Tokyo 113-0033 JP |
| Official Correspondent |
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| US Agent |
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| Registration Status | 1 |
| Initial Importer | N |
| Registration Expiration | 2020-04-25 |
| Registration Address | 3-5 Aza Yarokuuchi Inada Kasama Ibaraki, 309-1635 JP |
| Establishment Type | Manufacture Medical Device for Another Party (Contract Manufacturer) |
Device Company | Device | Date |
|---|---|---|
KAINOS LABORATORIES, INC., KASAMA FACTORY [KAINOS LABORATORIES INC] | Lucica Glycated Albumin-L | 2019-01-28 |
| NCAGE Code | SAFH0 | KAINOS LABORATORIES,INC. |
| CAGE Code | SAFH0 | KAINOS LABORATORIES,INC. |
| S.A.M. Registration | SAFH0 [691688980] | KAINOS LABORATORIES,INC. |