CURIDENT, LLC

FDA Device Registration & Listing · Boca Raton, FL, US · Registration 3043840120

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
3043840120
FEI Number
3043840120
Entity Name
CURIDENT, LLC
City/State/Country
Boca Raton, FL, US
Establishment Address
6790 E Rogers Cir, Boca Raton, FL 33487, US
Establishment Type(s)
Repack or Relabel Medical Device,Develop Specifications But Do Not Manufacture At This Facility
Owner / Operator
Curident, LLC (Owner Number: 10095512)
Owner / Operator Contact Address
6790 E rogers Circle, Boca Raton, FL 33487, 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 2026-03-23

Official Correspondent

Steven Zaken

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Curident, LLC
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 3043840120. Last updated year: 2026. Please use registration number 3043840120 when referencing this establishment in official correspondence.
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