FDA Device Entity Profile: Neurolief

Known Identifiers & Locations

FEI Numbers 3015088397, 3019551144

Owner Operator Numbers 10081665

Locations Covered Coral Springs, FL, US; Netanya Central, IL

Registered Establishments (2)

Registration #	Establishment Name	Location	Establishment Type(s)	Action
3015088397	NEUROLIEF Ltd.	Netanya Central, IL	Manufacture Medical Device,Export Device to the United States But Perform No Other Operation on Device,Complaint File Establishment per 21 CFR 820.198	View Details
3019551144	NEUROLIEF Inc.	Coral Springs, FL, US	Complaint File Establishment per 21 CFR 820.198	View Details

510(k) Premarket Notifications (0)

No 510(k) notifications found for this entity.

FDA Recall History (0)

No recall records found for this entity.

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