This page includes the latest FDA filings for Kainos Laboratories Inc Kasama Factory. Currently, you will find the latest 100 filings for Premarket Notifications, Premarket Applications, De Novo Applications, and GUDID registrations.
| 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 |