FILMART

FDA Device Registration & Listing · Brooklyn, NY, US · Registration 3011175600

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
3011175600
FEI Number
3011175600
Entity Name
FILMART
City/State/Country
Brooklyn, NY, US
Establishment Address
4724 18th Ave, Brooklyn, NY 11204, US
Establishment Type(s)
Repack or Relabel Medical Device
Owner / Operator
Filmart (Owner Number: 10047725)
Owner / Operator Contact Address
4724 18th Ave., Brooklyn, NY 11204, US
Initial Importer Flag
Y
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

No proprietary names listed under this establishment.

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
EFW Toothbrush, Manual Dental Class 1 872.6855 2014-10-23

Official Correspondent

No official correspondent registered.

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Filmart
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

Related 510(k) Records

510(k) Number Applicant Device Name Decision Date
K973236 Procter & Gamble Co. CREST TOOTHBRUSH WITH MICROSHIELD 1998-03-11

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3011175600. Last updated year: 2026. Please use registration number 3011175600 when referencing this establishment in official correspondence.
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