DILON MEDICAL TECHNOLOGIES, Inc

FDA Device Registration & Listing · Newport News, VA, US · Registration 3010060126

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
3010060126
FEI Number
3010060126
Entity Name
DILON MEDICAL TECHNOLOGIES, Inc
City/State/Country
Newport News, VA, US
Establishment Address
701 Mariners Row, Suite 200, Newport News, VA 23606, US
Establishment Type(s)
Complaint File Establishment per 21 CFR 820.198
Owner / Operator
Dilon Medical Technologies, Inc (Owner Number: 10042981)
Owner / Operator Contact Address
701 Mariners Row, Suite 200, Newport News, VA 23606, US
Initial Importer Flag
Y
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 2013-01-17

Official Correspondent

Pedro Cruz

US Agent Details

No US Agent registered (Local establishment).

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
3005755031 DILON MEDICAL TECHNOLOGIES LTD. Caesarea Haifa, IL

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3010060126. Last updated year: 2026. Please use registration number 3010060126 when referencing this establishment in official correspondence.
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