Nuline Sensors L L C

FDA Filings

This page includes the latest FDA filings for Nuline Sensors L L C. Currently, you will find the latest 100 filings for Premarket Notifications, Premarket Applications, De Novo Applications, and GUDID registrations.

FDA Registration(s)
Registration Number3010666140
FEI Number3010666140
NameNULINE SENSORS LLC
Owner & OperatorNuLine Sensors LLC
Contact Address210 Specialty Pt
Sanford FL 32771 US
Official Correspondent
  • James Monsor
  • 1-321-5371804-x
Registration Status1
Initial ImporterN
Registration Expiration2020-04-25
Registration Address210 Specialty Pt
Sanford, FL 32771 US
Establishment Type
  • Manufacture Medical Device
  • Develop Specifications But Do Not Manufacture At This Facility

FDA Filings

Device
Company
DeviceDate
NULINE SENSORS, LLC
 EKG Patch™ (Large) MGLRG2020-07-09
NULINE SENSORS, LLC
 EKG Patch™ (Medium) MGMED2020-07-09
NULINE SENSORS, LLC
 EKG Patch™ (Cable) MGCBLSP2020-07-09
NULINE SENSORS LLC
Cardiac Patch Cable2020-02-24
NULINE SENSORS LLC
InvisionHeart ECG System2017-12-14
NULINE SENSORS LLC
3 in 1 patch2017-12-14
NULINE SENSORS LLC
Patch Electrode2014-01-10

Related Finance Registrations
NCAGE Code74QV7NULINE SENSORS, LLC
CAGE Code74QV7NULINE SENSORS, LLC
DUNS079231054NULINE SENSORS, LLC
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