Data / Medical devices / Lubricant, Patient / United States
FDA-registered makers of Lubricant, Patient in the United States: 25 establishments
25 establishments in the United States are registered with the FDA to make Lubricant, Patient (product code KMJ). 7 have a 510(k) clearance or PMA approval on file and 1 has a recall event. FDA data exported November 2, 2026.
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- Device
- Lubricant, Patient
- Product code
- KMJ
- Country
- United States
Makers of Lubricant, Patient in the United States
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| MEDLINE INDUSTRIES, LP - Northfield | Northfield, IL, United States | Complaint file establishment, Specification developer | 3 | May 10, 2011 | 0 | 1 | 0 | api.fda.gov |
| Biofilm, Inc. | Vista, CA, United States | Manufacturer | 1 | February 18, 1994 | 0 | 0 | 0 | api.fda.gov |
| Greystone Medical, LLC | Waterford, MI, United States | Specification developer | 1 | April 10, 2012 | 0 | 0 | 0 | api.fda.gov |
| Nurse Assist, LLC | Haltom City, TX, United States | Manufacturer | 1 | August 10, 2012 | 0 | 0 | 0 | api.fda.gov |
| Parker Laboratories, Inc. | Fairfield, NJ, United States | Manufacturer | 1 | December 1, 1986 | 0 | 0 | 0 | api.fda.gov |
| Spirus Medical, LLC | W Bridgewater, MA, United States | Specification developer | 1 | April 3, 2008 | 0 | 0 | 0 | api.fda.gov |
| Wisconsin Pharmacal Co., LLC | Jackson, WI, United States | Manufacturer | 1 | October 26, 1990 | 0 | 0 | 0 | api.fda.gov |
| Advanced Cosmetic Research Laboratories Inc. | Chatsworth, CA, United States | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Arrow International LLC (subsidiary of Teleflex Incorporated) | Morrisville, NC, United States | Complaint file establishment, Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Biomed Laboratories LLC | Dallas, TX, United States | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Bioseal | Placentia, CA, United States | Contract manufacturer, Manufacturer, Repackager or relabeler | 0 | 0 | 0 | 0 | api.fda.gov | |
| Cosco International, Inc. | Marietta, GA, United States | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Cardinal Health | Hazelwood, MO, United States | Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Good Clean Love, Inc. | Eugene, OR, United States | Complaint file establishment, Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| HR PHARMACEUTICALS, INC d/b/a HR HealthCare | York, PA, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Impact Innovations LLC | Boca Raton, FL, United States | Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| LGM Pharma Solutions, LLC | Rosenberg, TX, United States | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Mayer Laboratories | Berkeley, CA, United States | Complaint file establishment, Repackager or relabeler, Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Pixie Cup LLC | Walnut Shade, MO, United States | Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Primo Medical Group, INC | Stoughton, MA, United States | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Primo Medical Group, Inc | W Bridgewater, MA, United States | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Ready Set Import | Beverly Hills, CA, United States | Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| SPAN PACKAGING SERVICES d.b.a. MULTI-PACK SOLUTIONS | Greenville, SC, United States | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| SWG Labs, Inc. dba Trigg Laboratories | Las Vegas, NV, United States | Contract manufacturer, Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Ulmer Pharmacal Co. | Park Rapids, MN, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov |
Updated November 2, 2026. 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.