Data / Medical devices / United States / Wisconsin Pharmacal Co., LLC
Wisconsin Pharmacal Co., LLC: FDA-registered device maker in Jackson, WI, United States, 4 510(k) clearances
Wisconsin Pharmacal Co., LLC is registered with the FDA (registration 2124143) in Jackson, WI, United States. It lists 4 device types. The FDA files 4 510(k) clearances under its listings, the newest dated January 9, 2020. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 2124143
- Address
- N 168 W 22223 Main ST, Jackson, WI, United States, 53037
- Owner or operator
- WISCONSIN PHARMACAL CO., LLC (2124143)
- Roles
- Complaint file establishment, Contract manufacturer, Manufacturer, Repackager or relabeler, Specification developer
- First device listed
- December 18, 2007
- Registered through
- 2026
- Brand names listed
- CVS Long-Lasting Moisturizing Vaginal Suppositories, CVS Personal Lubricant &Moisturizer, CVS Pharmacy Long-Lasting Feminine Moisturizer, Coleman 100 Piece Waterproof Kit, Coleman 200 Piece Expedition Kit, Coleman All Purpose Tin, Coleman Fishing Essentials Tin, Coleman Gift Pack First Aid Tins and more
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Dressing, Wound, Drug | FRO | U | Contract manufacturer, Manufacturer | accessdata.fda.gov |
| First Aid Kit With Drug | LRR | N | Complaint file establishment, Specification developer | accessdata.fda.gov |
| Lubricant, Patient | KMJ | 1 | Manufacturer | accessdata.fda.gov |
| Lubricant, Personal | NUC | 2 | Manufacturer, Repackager or relabeler | accessdata.fda.gov |
510(k) clearances
The 510(k) numbers this establishment lists, with the FDA decision on each. The applicant is the company that holds the clearance.
| Decided | 510(k) number | Device | Product code | Decision | Applicant | Source |
|---|---|---|---|---|---|---|
| January 9, 2020 | K191052 | HyaloGYN Vaginal Moisturizing Suppositories | NUC | Substantially Equivalent | Fidia Farmaceutici S.P.A. | accessdata.fda.gov |
| April 20, 2012 | K112666 | SALINE WOUND WASH | FRO | Substantially Equivalent | Nanoplas, Inc. | accessdata.fda.gov |
| April 4, 2007 | K062682 | CVS PERSONAL LUBRICANT AND MOISTURIZER | NUC | Substantially Equivalent | Lake Consumer Products, Inc. | accessdata.fda.gov |
| October 26, 1990 | K903910 | LUBRICATING JELLY | KMJ | Substantially Equivalent | Lake Pharmaceutical, Inc. | accessdata.fda.gov |
Compare with other makers
- All makers of Lubricant, Personal
- All makers of First Aid Kit With Drug
- All makers of Dressing, Wound, Drug
- All makers of Lubricant, Patient
Updated January 9, 2020. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.