Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3030089065

FEI Number

3030089065

Entity Name

TECHSOMED

City/State/Country

Or Yehuda Central, IL

Establishment Address

6 Ofra Haza St., Or Yehuda Central 6032303, IL

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

Techsomed (Owner Number: 10089374)

Owner / Operator Contact Address

Meir Weisgal 2, Rehovot, IL-D 7632605, IL

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

K243084

PMA Number

N/A

All Registered Proprietary Names

BioTrace.IO Precision 2

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
QZL	Post-Ablation Tissue Response Prediction Software	Radiology	Class 2	892.2052	2025-04-10

Official Correspondent

Dalia Dickman

US Agent Details

Stephen Lieberman Email: lieberman@donawa.com Phone: (561) 3020777

Related Public Records

Same Entity

Techsomed

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

View Entity Profile →

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3043617526	AD SCIENTIAM	Paris Ile-de-France, FR

Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3030089065. Last updated year: 2026. Please use registration number 3030089065 when referencing this establishment in official correspondence.