Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3009401421

FEI Number

3009401421

Entity Name

OPIA TECHNOLOGIES SAS

City/State/Country

Paris, FR

Establishment Address

17 Rue Moreau, Paris 75012, FR

Establishment Type(s)

Repack or Relabel Medical Device,Complaint File Establishment per 21 CFR 820.198,Develop Specifications But Do Not Manufacture At This Facility

Owner / Operator

Opia Technologies SAS (Owner Number: 10042009)

Owner / Operator Contact Address

17 Rue Moreau, Paris, FR-75 75012, FR

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

EYEPRIM

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
KET	Filters, Cell Collection, Tissue Processing	Pathology	Class 1	864.3010	2012-10-04

Official Correspondent

Pierre Roy

US Agent Details

DEBORAH NILSON Business: The Nilson Law Group PLLC Email: dnilson@nilsonlaw.com Phone: (212) 6871155

Related Public Records

Same Entity

Opia Technologies SAS

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

View Entity Profile →

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3009401421. Last updated year: 2026. Please use registration number 3009401421 when referencing this establishment in official correspondence.