Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

2124143

FEI Number

2124143

Entity Name

WISCONSIN PHARMACAL CO., LLC

City/State/Country

JACKSON, WI, US

Establishment Address

N 168 W 22223 MAIN ST, JACKSON, WI 53037, US

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

WISCONSIN PHARMACAL CO., LLC (Owner Number: 2124143)

Owner / Operator Contact Address

1 Pharmacal Way, --, Jackson, WI 53037, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

K903910

PMA Number

N/A

All Registered Proprietary Names

Steri-Wash Saline Wound Wash Encounter Personal Lubricant and Moisturizer H2O Pure Lube Personal Lubricant Fusion H2O Personal Lubricant CVS Personal Lubricant &Moisturizer Rite Aid Pharmacy Personal Lubricant and Moisturizer CVS Long-Lasting Moisturizing Vaginal Suppositories VagiGard Personal Lubricating Gel Walgreens Personal Lubricating Jelly CVS Pharmacy Long-Lasting Feminine Moisturizer Walgreens Long-Lasting Feminine Moisturizer

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
FRO	Dressing, Wound, Drug	Unknown	Class U	N/A	2018-07-25
NUC	Lubricant, Personal	Obstetrics/Gynecology	Class 2	884.5300	2007-12-18
NUC	Lubricant, Personal	Obstetrics/Gynecology	Class 2	884.5300	2023-04-14
KMJ	Lubricant, Patient	General Hospital	Class 1	880.6375	2007-12-18

Official Correspondent

Eileen Lolley

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

WISCONSIN PHARMACAL CO., 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
K150256	Argentum Medical	SILVERLON BURN CONTACT DRESSINGS	2015-04-30
K050212	Qualis, Inc.	PERSONAL WARMING JELLY	2005-03-17
K820587	Abco Dealers, Inc.	WET PACK LINE OF PRODUCTS	1982-03-26

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

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3043618351	NEORES D.O.O.	Mursko Sredisce Medimurska Zupanija, HR
3007128716	Medline Industries, LP	Norristown, PA, US
3012456427	UFP TECHNOLOGIES, INC.	Newburyport, MA, US
3019843904	OMEZA, LLC	Sarasota, FL, US

Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 2124143. Last updated year: 2026. Please use registration number 2124143 when referencing this establishment in official correspondence.