PLASTIC BILLAT

FDA Device Registration & Listing · GAMACHES Somme, FR · Registration 3032579800

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
3032579800
FEI Number
3032579800
Entity Name
PLASTIC BILLAT
City/State/Country
GAMACHES Somme, FR
Establishment Address
ZAE La Folie, GAMACHES Somme 80220, FR
Establishment Type(s)
Manufacture Medical Device for Another Party (Contract Manufacturer)
Owner / Operator
PLASTIC BILLAT (Owner Number: 10091380)
Owner / Operator Contact Address
ZAE La Folie, GAMACHES, FR-80 80220, FR
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

CLASSIC BY RISKONTROL ART BY RISKONTROL TOTAL PROTECT BY RISKONTROL

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
ECB Unit, Syringe, Air And/Or Water Dental Class 1 872.4565 2024-09-11

Official Correspondent

Mickael ROSANT

US Agent Details

Noelle Zuccarello Business: Acteon, Inc Email: noelle.zuccarello@acteongroup.com Phone: (800) 2896367

Related Public Records

Same Entity

PLASTIC BILLAT
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 3032579800. Last updated year: 2026. Please use registration number 3032579800 when referencing this establishment in official correspondence.
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