Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3013133723

FEI Number

3013133723

Entity Name

REDI-2-PAQ HOME PRODUCTS, LLC

City/State/Country

Sarasota, FL, US

Establishment Address

1712 Northgate Blvd, Sarasota, FL 34234, US

Establishment Type(s)

Manufacture Medical Device for Another Party (Contract Manufacturer)

Owner / Operator

Redi-2-PaQ Home Products, LLC (Owner Number: 10083184)

Owner / Operator Contact Address

1712 Northgate Blvd, Sarasota, FL 34234, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

Smilesaver Spearmint Spary 30 ml (1flo2) Omeza OCM Wound Care Matrix

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	2022-09-15
FRO	Dressing, Wound, Drug	Unknown	Class U	N/A	2021-11-01

Official Correspondent

No official correspondent registered.

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Redi-2-PaQ Home Products, 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
K902838	Denture Dynamic'S, Inc.	DENTURE DYNAMIC'S DENTURE MAGIC	1990-09-06
K150256	Argentum Medical	SILVERLON BURN CONTACT DRESSINGS	2015-04-30

Related Recall Records

Recall ID	Recalling Firm	Recall Class	Product Description
Z-0003-06	B. Braun Medical, Inc.	U	D-Stat Dry Hemostatic Bandage. The product is an adhesive bandage.
Z-0038-2025	3M Company Health Care Business 3m Center	U	3M Tegaderm CHG, Chlorhexidine Gluconate I.V. Securement Dressing, REF 1658R

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3009211643	WEIHAI HUIHAI COMMODITY MANUFACTURE CO., LTD.	Weihai Shandong, CN
1821514	KULZER, LLC	SOUTH BEND, IN, US

Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3013133723. Last updated year: 2026. Please use registration number 3013133723 when referencing this establishment in official correspondence.