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Data / Medical devices / Latex Patient Examination Glove / Indonesia

FDA-registered makers of Latex Patient Examination Glove in Indonesia: 7 establishments

7 establishments in Indonesia are registered with the FDA to make Latex Patient Examination Glove (product code LYY). 7 have a 510(k) clearance or PMA approval on file and 0 have a recall event. FDA data exported November 3, 2026.

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Device
Latex Patient Examination Glove
Product code
LYY
Country
Indonesia

Makers of Latex Patient Examination Glove in Indonesia

MakerLocationRole510(k) clearancesLatest clearancePMA approvalsRecall eventsClass ISource
Arista Latindo Industrial, Ltd. P.T.Jakarta Barat, IndonesiaManufacturer11October 21, 2002000api.fda.gov
Pt.shamrock Manufacturing Corp.MEDAN Sumatera Utara, IndonesiaManufacturer6May 20, 2008000api.fda.gov
P.T. Maja Agung LatexindoSUNGGAL DELI SERDANG Sumatera Utara, IndonesiaManufacturer4August 28, 2008000api.fda.gov
PT. Intan Hevea IndustryMEDAN Sumatera Utara, IndonesiaContract manufacturer, Manufacturer, Specification developer3November 4, 2011000api.fda.gov
PT. Medisafe TechnologiesKab. Deli Serdang Sumatera Utara, IndonesiaContract manufacturer, Manufacturer3March 19, 1999000api.fda.gov
PT. Universal GlovesMEDAN Sumatera Utara, IndonesiaManufacturer2November 19, 2021000api.fda.gov
PT. Haloni JaneCIKUPA, TANGERANG Banten, IndonesiaManufacturer1November 9, 2006000api.fda.gov

Updated November 3, 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.