Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3022133572

FEI Number

3022133572

Entity Name

LAVIOR PHARMA INC.

City/State/Country

Hallandale Beach, FL, US

Establishment Address

1250 E Hallandale Beach Blvd Ste 302, Hallandale Beach, FL 33009, US

Establishment Type(s)

Manufacture Device in the United States for Export Only

Owner / Operator

Lavior Pharma Inc. (Owner Number: 10086490)

Owner / Operator Contact Address

1250 E Hallandale Beach Blvd, Suite 302, Hallandale Beach, FL 33009, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

Diabetic Itch Shield Skin Barrier Cream Diabetic Wound Therapy Advanced Dermal Barrier Cream Advanced Post-Procedure Barrier Gel Hydrogel Wound Dressing Diabetic Hydrogel Wound Dressing Diabetic Skin Barrier Cream Advanced Diabetic Wound Hydrogel Advanced Itch & Irritation Barrier Cream Itch Shield Skin Barrier Cream Post-Surgical Skin Barrier Gel Advanced MultiCare Hydrogel Multipupose Wound Gel OatShield Skin Barrier Cream

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
NAE	Dressing, Wound, Hydrogel Without Drug And/Or Biologic	General, Plastic Surgery	Class 1	878.4022	2022-11-14
FRO	Dressing, Wound, Drug	Unknown	Class U	N/A	2025-07-10

Official Correspondent

Anabelle Savion

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Lavior Pharma 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
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

Similar Registrations

Registration Number	Establishment Name	Location
3009662219	Custom Medical and Safety Products Inc.	Buffalo, NY, US
3038014307	CURAPEP LLC	Burlington, WI, US
3043012215	ZENESIS HOLDINGS CO., LIMITED	Kowloon, HK
3008646686	KIKGEL	Ujazd Opolskie, PL
8043484	Smith & Nephew Medical Ltd	HULL East Riding of Yorkshire, GB

Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3022133572. Last updated year: 2026. Please use registration number 3022133572 when referencing this establishment in official correspondence.