This page includes the latest FDA filings for Junopacific Inc. Currently, you will find the latest 100 filings for Premarket Notifications, Premarket Applications, De Novo Applications, and GUDID registrations.
Registration Number | 3007867826 |
FEI Number | 3007867826 |
Name | JunoPacific Inc. |
Owner & Operator | JunoPacific Inc. |
Contact Address | 2840 Research Park Drive Soquel CA 95073 US |
Official Correspondent |
|
Registration Status | 1 |
Initial Importer | N |
Registration Expiration | 2020-04-25 |
Registration Address | 2840 Research Park Dr Soquel, CA 95073 US |
Establishment Type | Manufacture Medical Device for Another Party (Contract Manufacturer) |
Registration Number | 2134604 |
FEI Number | 3002623849 |
Name | JUNOPACIFIC INC. |
Owner & Operator | JUNOPACIFIC INC. |
Contact Address | 1040 Lund Blvd. -- Anoka MN 55303 US |
Official Correspondent |
|
Registration Status | 1 |
Initial Importer | N |
Registration Expiration | 2020-04-25 |
Registration Address | 1040 Lund Blvd ANOKA, MN 55303 US |
Establishment Type | Manufacture Medical Device for Another Party (Contract Manufacturer) |
Device Company | Device | Date |
---|---|---|
JunoPacific Inc. | Catalys? Precision Laser System | 2020-02-21 |
JUNOPACIFIC INC. | Soma Access Systems ExactTrack I Procedure Kit | 2012-10-05 |
JUNOPACIFIC INC. | Soma Access Systems ExactTrack I Procedure Kit | 2012-10-05 |