Skip to the page

Data / Medical devices / Malaysia / Yty Acheh

Yty Acheh: FDA-registered device maker in Sitiawan Perak, Malaysia, 6 510(k) clearances

Yty Acheh is registered with the FDA (registration 3014847584) in Sitiawan Perak, Malaysia. It lists 4 device types. The FDA files 6 510(k) clearances under its listings, the newest dated September 27, 2024. Registered through 2027. 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
3014847584
Address
Lot 15651, Kawasan Perindustrian Kampung Acheh, Sitiawan Perak, Malaysia, 32000
Owner or operator
YTY Acheh (10058255)
Roles
Contract manufacturer, Manufacturer
First device listed
August 8, 2018
Registered through
2027
Brand names listed
Purple 9.5

Devices it lists

DeviceProduct codeClassRoleSource
Fentanyl And Other Opioid Protection GloveQDO1Contract manufacturer, Manufactureraccessdata.fda.gov
Medical Glove, SpecialtyLZC1Contract manufacturer, Manufactureraccessdata.fda.gov
Medical Gloves With Chemotherapy Labeling Claims - Test For Use With Chemotherapy DrugsOPJ1Contract manufacturer, Manufactureraccessdata.fda.gov
Polymer Patient Examination GloveLZA1Contract manufacturer, 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
September 27, 2024K241909Halyard Purple Nitrile* Powder-Free Exam Gloves, Low Dermatitis Potential, Tested for Use with Chemotherapy Drugs, Fentanyl Citrate, Simulated Gastric Acid and Fentanyl in Simulated Gastric AcidLZASubstantially EquivalentO&M Halyard, Inc.accessdata.fda.gov
June 27, 2018K180646Halyard Lavender Nitrile Powder-Free Exam Glove Tested for Use with Chemotherapy DrugsLZCSubstantially EquivalentHalyard Healthaccessdata.fda.gov
August 25, 2017K171104Non-Sterile, Powder Free Nitrile Examination Gloves, Tested for use with Chemotherapy Drugs (Blue, Cobalt Blue)LZASubstantially EquivalentYty Industry (Manjung) Sdn Bhdaccessdata.fda.gov
January 16, 2015K142283Non-Sterile, Powder Free Nitrile Examination Gloves (Blue, Black and White Color)LZASubstantially EquivalentYty Industry (Manjung) Sdn Bhdaccessdata.fda.gov
July 21, 2010K101596KIMBERLY-CLARK PURPLE NITRILE POWDER-FREE EXAM GLOVE (CHEMOTHERAPY GLOVE) AND KIMBERLY-CLARK PURPLE NITRILE XTRA POWDER-LZCSubstantially EquivalentKimberly-Clarkaccessdata.fda.gov
July 14, 2008K081089KIMBERLY-CLARK STERLING NITRILE & NITRILE-XTRA POWDER-FREE EXAM GLOVES WITH CHEMOTHERAPY DRUG USE CLAIMLZCSubstantially EquivalentKimberly-Clark Corp.accessdata.fda.gov

Compare with other makers

Updated September 27, 2024. 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.