Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3023339162

FEI Number

3023339162

Entity Name

ZSQUARE LTD

City/State/Country

Petah Tikva Central, IL

Establishment Address

43 Hasivim St. Petah Tikva 4959501, Israel, Petah Tikva Central 4959501, IL

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

Zsquare LTD (Owner Number: 10085636)

Owner / Operator Contact Address

43 Hasivim St. Petah Tikva 4959501, Israel, Petah Tikva, IL-M 4959501, IL

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

K220004

PMA Number

N/A

All Registered Proprietary Names

Zsqaure ENT-Flex Endoscope

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
EOB	Nasopharyngoscope (Flexible Or Rigid)	Ear, Nose, Throat	Class 2	874.4760	2022-07-13

Official Correspondent

Evgeny Bruhin

US Agent Details

Jerry Doane Business: FDAbasics Email: usagent@fdabasics.com Phone: (716) 7750533

Related Public Records

Same Entity

Zsquare LTD

View consolidated registration, premarket clearance, and recall records for this applicant.

View Entity Profile →

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3023339162. Last updated year: 2026. Please use registration number 3023339162 when referencing this establishment in official correspondence.