Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

2435952

FEI Number

1000137415

Entity Name

PROTECH PROFESSIONAL PRODUCTS, INC.

City/State/Country

BOYNTON BEACH, FL, US

Establishment Address

2900 Commerce Park Dr Ste 10, BOYNTON BEACH, FL 33426, US

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

PROTECH PROFESSIONAL PRODUCTS, INC. (Owner Number: 9006187)

Owner / Operator Contact Address

2900 NW COMMERCE PARK DR., #10, Boynton Beach, FL 33426, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

SMILE AGAIN PROTECH CONCENTRAT

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	2003-09-15

Official Correspondent

RANDI BLOCH

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

PROTECH PROFESSIONAL PRODUCTS, 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 2435952. Last updated year: 2026. Please use registration number 2435952 when referencing this establishment in official correspondence.