NANOVIBRONIX, LTD.

FDA Device Registration & Listing · NESHER Haifa, IL · Registration 3006262007

Public Record Device Listing Expiry Year: 2026 This page presents structured fields from public FDA datasets.

Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source
FDA Device Registration & Listing
Record Type
Device registration/listing
Registration Number
3006262007
FEI Number
3006262007
Entity Name
NANOVIBRONIX, LTD.
City/State/Country
NESHER Haifa, IL
Establishment Address
47, Ha-Ta'Asiya, NESHER Haifa 3688847, IL
Establishment Type(s)
Develop Specifications But Do Not Manufacture At This Facility
Owner / Operator
NANOVIBRONIX, LTD. (Owner Number: 9102520)
Owner / Operator Contact Address
47 HaTa'asiya St., --, NESHER, IL-NOTA 3688847, IL
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
PMA Number
N/A

All Registered Proprietary Names

PainShield MD

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
PFW Stationary Ultrasonic Diathermy Device For Use In Applying Therapeutic Deep Heat Physical Medicine Class 2 890.5300 2008-09-16

Official Correspondent

No official correspondent registered.

US Agent Details

Thomas Dold Business: Nanovibronix, Inc Email: tomd@NANOVIBRONIX.COM Phone: (612) 9656057

Related Public Records

Same Entity

NANOVIBRONIX, LTD.
View consolidated registration, premarket clearance, and recall records for this applicant.
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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3006262007. Last updated year: 2026. Please use registration number 3006262007 when referencing this establishment in official correspondence.
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