Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3006701790

FEI Number

3006701790

Entity Name

BeamMed Ltd.

City/State/Country

Petah Tikva Central, IL

Establishment Address

8 Ha-Lapid Street, Petah Tikva Central 4925822, IL

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

BeamMed Ltd (Owner Number: 10024010)

Owner / Operator Contact Address

8 Halapid Street, Petah Tikva, Petah Tikva, IL-TA 49710, IL

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

K110646

PMA Number

N/A

All Registered Proprietary Names

Sunlight MiniOmni

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
MUA	Bone Sonometer	Radiology	Class 2	892.1180	2011-11-23

Official Correspondent

Tal Marom

US Agent Details

Gilad Zamir Business: Beammed Email: gilad@beammed.com Phone: (800) 7696808

Related Public Records

Same Entity

BeamMed Ltd

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

View Entity Profile →

Related 510(k) Records

510(k) Number	Applicant	Device Name	Decision Date
K161919	Cyberlogic, Inc.	UltraScan 650	2017-04-05

Similar Registrations

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9710602	GE MEDICAL SYSTEMS (CHINA) CO., LTD.	WUXI Jiangsu, CN
3028606342	OMAY(GUANGZHOU) MED TECHNOLOGIES CO., LTD	Guangzhou Guangdong, CN

Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3006701790. Last updated year: 2026. Please use registration number 3006701790 when referencing this establishment in official correspondence.