ODC INDUSTRIES

FDA Device Registration & Listing · Ploermel Bretagne, FR · Registration 3015427564

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
3015427564
FEI Number
3015427564
Entity Name
ODC INDUSTRIES
City/State/Country
Ploermel Bretagne, FR
Establishment Address
Rue Thomas Edison, ZA du Bois vert, Ploermel Bretagne 56800, FR
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
ODC Industries (Owner Number: 10094516)
Owner / Operator Contact Address
Rue Thomas Edison, ZA du Bois vert, Ploermel, FR-NOTA 56800, FR
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

ScleralEase

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
KYE Inserter/Remover Contact Lens Ophthalmic Class 1 886.5420 2025-12-04

Official Correspondent

Fabien Martin

US Agent Details

Bret Andre Business: EYEREG CONSULTING INC. Email: bandre@fdapproval.com Phone: (503) 3725226

Related Public Records

Same Entity

ODC Industries
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 3015427564. Last updated year: 2026. Please use registration number 3015427564 when referencing this establishment in official correspondence.
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