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 |