This page includes the latest FDA filings for Soonsolid. Currently, you will find the latest 100 filings for Premarket Notifications, Premarket Applications, De Novo Applications, and GUDID registrations.
Registration Number | 0 |
FEI Number | 0 |
Name | Soonsolid |
Owner & Operator | SprintRay Inc. |
Contact Address | 2705 Media Center Drive Los Angeles CA 90065 US |
Official Correspondent |
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US Agent |
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Registration Status | 5 |
Initial Importer | N |
Registration Expiration | 2020-04-25 |
Registration Address | 4th Floor, No.2 Qihang Building, Sci.&Tech. Park, NO.586 Xihuan Road, Keqiao District Shaoxing Zhejiang, 00000 CN |
Establishment Type | Manufacture Medical Device |
Device Company | Device | Date |
---|---|---|
Soonsolid [SprintRay Inc.] | CF2000, Swab Resin | 2020-03-31 |
Soonsolid [SprintRay Inc.] | SprintRay SG Resin | 2019-02-01 |
Soonsolid [SprintRay Inc.] | SprintRay Try-in | 2019-02-01 |
Soonsolid [SprintRay Inc.] | SprintRay IDBT | 2019-02-01 |
Soonsolid [SprintRay Inc.] | SprintRay Ortho Clear | 2019-02-01 |