This page includes the latest FDA filings for Asahi Intecc Usa Inc. Currently, you will find the latest 100 filings for Premarket Notifications, Premarket Applications, De Novo Applications, and GUDID registrations.
Asahi Intecc Usa Inc holds import registrations or U.S. agent authorizations in conjunction with the following organizations:
| Registration Number | 3004718255 |
| FEI Number | 3004718255 |
| Name | ASAHI INTECC USA, INC. |
| Owner & Operator | ASAHI INTECC CO., LTD. |
| Contact Address | 3-100 Akatsuki-cho -- Seto JP-23 Aiti 489-0071 JP |
| Registration Status | 1 |
| Initial Importer | Y |
| Registration Expiration | 2020-04-25 |
| Registration Address | 3002 Dow Ave Suite 212 Tustin, CA 92780 US |
| Establishment Type | Develop Specifications But Do Not Manufacture At This Facility |
Device Company | Device | Date |
|---|---|---|
ASAHI INTECC USA, INC. [ASAHI INTECC CO., LTD.] | ASAHI CROSSWALK Peripheral Support Catheter | 2019-12-02 |
ASAHI INTECC USA, INC. | ASAHI TREASURE FLOPPY PERIPHERAL GUIDE WIRE | 2011-03-18 |
| NCAGE Code | 39GN3 | ASAHI INTECC USA, INC. |
| CAGE Code | 39GN3 | ASAHI INTECC USA, INC. |
| S.A.M. Registration | 39GN3 [102886491] | ASAHI INTECC USA, INC. |