DILON TECHNOLOGIES INC

FDA Device Registration & Listing · NEWPORT NEWS, VA, US · Registration 1125612

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
1125612
FEI Number
3002931663
Entity Name
DILON TECHNOLOGIES INC
City/State/Country
NEWPORT NEWS, VA, US
Establishment Address
701 Mariners Row, Suite 200, NEWPORT NEWS, VA 23606, US
Establishment Type(s)
Manufacture Medical Device,Develop Specifications But Do Not Manufacture At This Facility
Owner / Operator
DILON TECHNOLOGIES Inc (Owner Number: 9035906)
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
N/A

All Registered Proprietary Names

HEMOBLAST™ Bellows CoPilot VL

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
PMX Absorbable Collagen Hemostatic Agent With Thrombin General, Plastic Surgery Class 3 878.4490 2022-10-17
CCW Laryngoscope, Rigid Anesthesiology Class 1 868.5540 2018-11-14

Official Correspondent

Pedro Cruz

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

DILON 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
3007702492 Dilon Technologies France SAS St Priest Rhone, FR

Related Recall Records

Recall ID Recalling Firm Recall Class Product Description
Z-0144-2024 Covidien 1
Stolen McGRATH MAC Video Laryngoscopes, REF: 301-000-000
Z-0168-2024 Covidien 1
McGrath Mac 2, Disposable Laryngoscope Blade, REF: 350-017-000, Sterile EO, Rx Only
Z-0169-2024 Covidien 1
McGrath Mac 2, Disposable Laryngoscope Blade, REF: 350-084-000, Sterile EO, Rx Only

Similar Registrations

Registration Number Establishment Name Location
2011171 Sterigenics US LLC Los Angeles, CA, US
3035387162 NAS MED LLC FZ DUBAI Dubayy, AE
3007702492 Dilon Technologies France SAS St Priest Rhone, FR
1416980 BAXTER HEALTHCARE CORPORATION ROUND LAKE, IL, US
3010162973 Synergy Health Marseille SAS MARSEILLE CEDEX 14 Provence-Alpes-Cote d'Azur, FR
Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 1125612. Last updated year: 2026. Please use registration number 1125612 when referencing this establishment in official correspondence.
Legal Disclaimer: AvaSpecs is not affiliated with the FDA or any government agency and does not provide medical, legal, regulatory, safety, approval, clearance, effectiveness, endorsement, or compliance advice. This index page is built using public record archives and does not represent an official regulatory determination.
Account Required Full available specs will require a free AvaSpecs account.