REGENT LABS, INC.

FDA Device Registration & Listing · Deerfield Bch, FL, US · Registration 1058743

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
1058743
FEI Number
1000307739
Entity Name
REGENT LABS, INC.
City/State/Country
Deerfield Bch, FL, US
Establishment Address
473 GOOLSBY BLVD., Deerfield Bch, FL 33442, US
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
REGENT LABS, INC. (Owner Number: 9023971)
Owner / Operator Contact Address
473 GOOLSBY BLVD., Deerfield Beach, FL 33442, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

STAIN AWAY PLUS KLEENITE

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
EFT Cleanser, Denture, Over The Counter Dental Class 1 872.3520 1995-12-27

Official Correspondent

RANDALL RE

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

REGENT LABS, INC.
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
K902838 Denture Dynamic'S, Inc. DENTURE DYNAMIC'S DENTURE MAGIC 1990-09-06

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 1058743. Last updated year: 2026. Please use registration number 1058743 when referencing this establishment in official correspondence.
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