Dilon Technologies France SAS

FDA Device Registration & Listing · St Priest Rhone, FR · Registration 3007702492

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
3007702492
FEI Number
3007702492
Entity Name
Dilon Technologies France SAS
City/State/Country
St Priest Rhone, FR
Establishment Address
8 Allee Irene Joliot Curie, St Priest Rhone 69800, FR
Establishment Type(s)
Repack or Relabel Medical Device,Manufacture Medical Device
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
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number

All Registered Proprietary Names

HEMOBLAST™ Bellows

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

Official Correspondent

Pedro Cruz

US Agent Details

Pedro Cruz Business: Dilon Technologies Email: pcruz@dilon.com Phone: (321) 6173501

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
1125612 DILON TECHNOLOGIES INC NEWPORT NEWS, VA, US

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3007702492. Last updated year: 2026. Please use registration number 3007702492 when referencing this establishment in official correspondence.
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