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PT Healthguard Technologies: FDA-registered device maker in Simalungun Sumatera Utara, Indonesia, 2 510(k) clearances

PT Healthguard Technologies is registered with the FDA (registration 3038187456) in Simalungun Sumatera Utara, Indonesia. It lists 4 device types. The FDA files 2 510(k) clearances under its listings, the newest dated February 18, 2025. Registered through 2026. FDA data exported November 2, 2026.

SpecStream is the live web data engine for teams and agents. It reads the FDA registration and listing, 510(k), PMA, recall and enforcement files from openFDA every week, and this page is that reading, joined by the FDA's own numbers. Ask for the makers of any device type in any country and new clearances, approvals and recalls arrive in your sheet, CRM, Slack or agent as the FDA publishes them.

FDA registration number
3038187456
Address
Jalan Surfaktan Kavling E28, Sei Mangkei, Desa/Kelurahan Kec. Bosar Maligas, Kab., Simalungun Sumatera Utara, Indonesia, 21183
Owner or operator
PT HealthGuard Technologies (10093198)
Roles
Contract manufacturer, Exporter to the US, Manufacturer
First device listed
April 13, 2025
Registered through
2026
Brand names listed
Nitrile Powder-Free Exam Gloves Tested for Use with Chemotherapy Drugs, Nitrile Powder-Free Exam Gloves Tested for Use with Chemotherapy Drugs, Opioid Fentanyl Citrate, Simulated Gastric Acid, Nitrile examination glove

Devices it lists

DeviceProduct codeClassRoleSource
Fentanyl And Other Opioid Protection GloveQDO1Exporter to the US, Manufactureraccessdata.fda.gov
Medical Glove, SpecialtyLZC1Exporter to the US, Manufactureraccessdata.fda.gov
Medical Gloves With Chemotherapy Labeling Claims - Test For Use With Chemotherapy DrugsOPJ1Contract manufacturer, Exporter to the US, Manufactureraccessdata.fda.gov
Polymer Patient Examination GloveLZA1Contract manufacturer, Exporter to the US, Manufactureraccessdata.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.

Decided510(k) numberDeviceProduct codeDecisionApplicantSource
February 18, 2025K243792Nitrile Powder-Free Exam Gloves Tested for Use with Chemotherapy Drugs, Opioid Fentanyl Citrate (Black,White)LZASubstantially EquivalentBasic Medical Technology, Inc.accessdata.fda.gov
January 31, 2025K243441Nitrile Powder-Free Exam Gloves Tested for Use with Chemotherapy Drugs, Opioid Fentanyl Citrate, Simulated Gastric Acid (Light blue, Dark blue)LZASubstantially EquivalentBasic Medical Technology, Inc.accessdata.fda.gov

Compare with other makers

Updated February 18, 2025. 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.