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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

MakerLocationRole510(k) clearancesLatest clearancePMA approvalsRecall eventsClass ISource
MEDLINE INDUSTRIES, LP - NorthfieldNorthfield, IL, United StatesComplaint file establishment, Specification developer3May 10, 2011010api.fda.gov
Biofilm, Inc.Vista, CA, United StatesManufacturer1February 18, 1994000api.fda.gov
Greystone Medical, LLCWaterford, MI, United StatesSpecification developer1April 10, 2012000api.fda.gov
Nurse Assist, LLCHaltom City, TX, United StatesManufacturer1August 10, 2012000api.fda.gov
Parker Laboratories, Inc.Fairfield, NJ, United StatesManufacturer1December 1, 1986000api.fda.gov
Spirus Medical, LLCW Bridgewater, MA, United StatesSpecification developer1April 3, 2008000api.fda.gov
Wisconsin Pharmacal Co., LLCJackson, WI, United StatesManufacturer1October 26, 1990000api.fda.gov
Advanced Cosmetic Research Laboratories Inc.Chatsworth, CA, United StatesContract manufacturer0000api.fda.gov
Arrow International LLC (subsidiary of Teleflex Incorporated)Morrisville, NC, United StatesComplaint file establishment, Specification developer0000api.fda.gov
Biomed Laboratories LLCDallas, TX, United StatesContract manufacturer0000api.fda.gov
BiosealPlacentia, CA, United StatesContract manufacturer, Manufacturer, Repackager or relabeler0000api.fda.gov
Cosco International, Inc.Marietta, GA, United StatesContract manufacturer0000api.fda.gov
Cardinal HealthHazelwood, MO, United StatesSpecification developer0000api.fda.gov
Good Clean Love, Inc.Eugene, OR, United StatesComplaint file establishment, Specification developer0000api.fda.gov
HR PHARMACEUTICALS, INC d/b/a HR HealthCareYork, PA, United StatesManufacturer0000api.fda.gov
Impact Innovations LLCBoca Raton, FL, United StatesSpecification developer0000api.fda.gov
LGM Pharma Solutions, LLCRosenberg, TX, United StatesContract manufacturer0000api.fda.gov
Mayer LaboratoriesBerkeley, CA, United StatesComplaint file establishment, Repackager or relabeler, Specification developer0000api.fda.gov
Pixie Cup LLCWalnut Shade, MO, United StatesSpecification developer0000api.fda.gov
Primo Medical Group, INCStoughton, MA, United StatesContract manufacturer0000api.fda.gov
Primo Medical Group, IncW Bridgewater, MA, United StatesContract manufacturer0000api.fda.gov
Ready Set ImportBeverly Hills, CA, United StatesSpecification developer0000api.fda.gov
SPAN PACKAGING SERVICES d.b.a. MULTI-PACK SOLUTIONSGreenville, SC, United StatesContract manufacturer0000api.fda.gov
SWG Labs, Inc. dba Trigg LaboratoriesLas Vegas, NV, United StatesContract manufacturer, Manufacturer0000api.fda.gov
Ulmer Pharmacal Co.Park Rapids, MN, United StatesManufacturer0000api.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.