This page includes the latest FDA filings for Curvebeam. Currently, you will find the latest 100 filings for Premarket Notifications, Premarket Applications, De Novo Applications, and GUDID registrations.
Registration Number | 3009543051 |
FEI Number | 3009543051 |
Name | CurveBeam, LLC |
Owner & Operator | CurveBeam |
Contact Address | 2800 Bronze Dr. STE#110 Hatfield PA 19440 US |
Registration Status | 1 |
Initial Importer | N |
Registration Expiration | 2020-04-25 |
Registration Address | 2800 Bronze Dr. STE#110 Hatfield, PA 19440 US |
Establishment Type | Manufacture Medical Device |
Device Company | Device | Date |
---|---|---|
CurveBeam, LLC [CurveBeam] | CubeVue | 2018-09-05 |
CurveBeam, LLC [CurveBeam] | pedCAT Premium | 2018-06-20 |
CurveBeam, LLC [CurveBeam] | LineUP | 2018-06-20 |
CurveBeam, LLC [CurveBeam] | Strax HR-pQCT | 2017-06-15 |
CurveBeam, LLC [CurveBeam] | In Reach | 2017-06-15 |
CurveBeam, LLC [CurveBeam] | PedCAT | 2012-04-16 |
CurveBeam, LLC [CurveBeam] | PedCAT | 2012-04-16 |
Import ID | Shipment | Cargo Description | Quantity |
---|---|---|---|
2019122840325 | Barcadera,Aruba -> Port Everglades, Florida | SNAPPY SCREEN | 1 PCS |
2019122036649 | Puerto Cabello ,Venezuala -> Port Everglades, Florida | SNAPPY SCREEN | 1 PCS |