Uvision360 Inc

FDA Filings

This page includes the latest FDA filings for Uvision360 Inc. Currently, you will find the latest 100 filings for Premarket Notifications, Premarket Applications, De Novo Applications, and GUDID registrations.

FDA Registration(s)
Registration Number3014834623
FEI Number3014834623
NameUVISION360, INC.
Owner & OperatorUVision360, Inc.
Contact Address158 Wind Chime Court Suite #201
Raleigh NC 27615 US
Official Correspondent
  • Allison London Brown
  • 1-888-8559360-x
Registration Status1
Initial ImporterN
Registration Expiration2020-04-25
Registration Address158 Wind Chime Court Suite #201
Raleigh, NC 27615 US
Establishment TypeDevelop Specifications But Do Not Manufacture At This Facility

FDA Filings

Device
Company
DeviceDate
Uvision360, Inc.
LUMINELLE DTx System2021-06-30
UVISION360, INC.
LUMINELLE Dx 360 Rotatable Disposable Sheath (Diagnostic)2019-11-04
UVISION360, INC.
LUMINELLE Dx 360 Rotatable Disposable Sheath (Diagnostic)2019-11-04
UVision360 Inc.
Luminelle DTx Hysteroscopy System, Luminelle Dx 360 Rotatable Disposable Sheath (Diagnostic)2019-11-01
UVISION360, INC.
LUMINELLE DTx Hysteroscopy System2019-06-13
UVISION360, INC.
LUMINELLE DTx Hysteroscopy System2019-06-13
UVision360 Inc.
Luminelle DTx Hysteroscopy System, Luminelle 360 Rotatable Sterile Disposable Sheath Rigid2019-06-06
UVISION360, INC.
LUMINELLE DTx Hysteroscopy System2018-10-18
UVISION360, INC.
LUMINELLE DTx Hysteroscopy System2018-10-18
UVision360 Inc.
Luminelle DTx Hysteroscopy System2018-08-16

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