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Data / Medical devices / Latex Patient Examination Glove / United States

FDA-registered makers of Latex Patient Examination Glove in the United States: 18 establishments

18 establishments in the United States are registered with the FDA to make Latex Patient Examination Glove (product code LYY). 17 have a 510(k) clearance or PMA approval on file and 2 have a recall event. FDA data exported November 2, 2026.

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Device
Latex Patient Examination Glove
Product code
LYY
Country
United States

Makers of Latex Patient Examination Glove in the United States

MakerLocationRole510(k) clearancesLatest clearancePMA approvalsRecall eventsClass ISource
Ansell Healthcare Products LLCReno, NV, United StatesManufacturer, Specification developer30August 20, 2021010api.fda.gov
Haywood Vocational Opportunities Inc.Waynesville, NC, United StatesContract manufacturer, Repackager or relabeler9March 23, 2011000api.fda.gov
Mexpo International, Inc.Union City, CA, United StatesContract manufacturer, Manufacturer9March 6, 2015000api.fda.gov
SW Technologies Inc.Union City, CA, United StatesManufacturer7September 23, 2002000api.fda.gov
Bay MedicalBrisbane, CA, United StatesSpecification developer2November 30, 1998000api.fda.gov
Mayer LaboratoriesBerkeley, CA, United StatesRepackager or relabeler, Specification developer2November 29, 2001000api.fda.gov
MEDLINE INDUSTRIES, LP - NorthfieldNorthfield, IL, United StatesComplaint file establishment, Specification developer2May 23, 2017000api.fda.gov
American Healthcare Products, Inc.Alhambra, CA, United StatesSpecification developer1February 4, 1999010api.fda.gov
Ansell Healthcare Products LLCIselin, NJ, United StatesSpecification developer1August 20, 2021000api.fda.gov
Ascend Eagle, Inc.Pinole, CA, United StatesSpecification developer1January 25, 2006000api.fda.gov
Gel-X LLCWilmington, DE, United StatesManufacturer, Specification developer1July 24, 2013000api.fda.gov
Icp, Inc.Green Bay, WI, United StatesSpecification developer1May 11, 2017000api.fda.gov
Ims, Inc.Bixby, OK, United StatesSpecification developer1June 26, 2003000api.fda.gov
Labsource, IncNorthlake, IL, United StatesSpecification developer1April 23, 1998000api.fda.gov
Medical University Hospital AuthorityNorth Charleston, SC, United StatesManufacturer1May 6, 1997000api.fda.gov
Nucare LLCMontclair, CA, United StatesSpecification developer1June 9, 1998000api.fda.gov
Ug Healthcare (usa), Inc.Costa Mesa, CA, United StatesSpecification developer1November 30, 2006000api.fda.gov
A-1 Creative Packaging LLCFort Atkinson, WI, United StatesContract manufacturer0000api.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.