Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3005755031

FEI Number

3005755031

Entity Name

DILON MEDICAL TECHNOLOGIES LTD.

City/State/Country

Caesarea Haifa, IL

Establishment Address

20 Alon Hatavor St., P.O.Box 3131, Caesarea Haifa 3079519, IL

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

Dilon Medical Technologies, Inc (Owner Number: 10042864)

Owner / Operator Contact Address

701 Mariners Row, Suite 200, Newport News, VA 23606, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

P110014

All Registered Proprietary Names

MarginProbe Probe MarginProbe System MarginProbe Console

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
OEE	Diagnostic Low Electric Field	Unknown	Class 3	N/A	2013-01-08

Official Correspondent

Pedro Cruz

US Agent Details

Pedro Cruz Business: DILON MEDICAL TECHNOLOGIES, INC Email: pcruz@dilon.com Phone: (321) 6173501

Related Public Records

Same Entity

Dilon Medical Technologies, Inc

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

View Entity Profile →

Other Registrations for Same Entity

Registration Number	Establishment Name	Location
3010060126	DILON MEDICAL TECHNOLOGIES, Inc	Newport News, VA, US

Similar Registrations

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3010060126	DILON MEDICAL TECHNOLOGIES, Inc	Newport News, VA, US
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3031365458	WOMED SAS	Montpellier Herault, FR
3009999323	STORE-ALL LOGISTICS LTD	Slieverue Kilkenny, IE
3008478369	FERROSAN MEDICAL DEVICES A/S	Soeborg Hovedstaden, DK

Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3005755031. Last updated year: 2026. Please use registration number 3005755031 when referencing this establishment in official correspondence.