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Data / Medical devices / Malaysia / Creative Contract (M) Sdn Bhd

Creative Contract (M) Sdn Bhd: FDA-registered device maker in Klang Selangor, Malaysia, 1 510(k) clearance

Creative Contract (M) Sdn Bhd is registered with the FDA (registration 9680409) in Klang Selangor, Malaysia. It lists 1 device type. The FDA files 1 510(k) clearance under its listings, the newest dated March 5, 2003. 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
9680409
FEI number
3007837161
Address
Kilang Medicos, Lot 2729, Jalan Gendang /KS2, Taman Perindustrian Klang Jaya, Bandar Diraja Klang, Klang Selangor, Malaysia, 41200
Owner or operator
CREATIVE CONTRACT (M) SDN BHD (9008799)
Roles
Contract manufacturer, Manufacturer
First device listed
February 22, 1994
Registered through
2026

Devices it lists

DeviceProduct codeClassRoleSource
Mask, SurgicalFXX2Contract 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
March 5, 2003K021533DERMASSIST PROCEDURE MASK/SURGICAL MASKS (GREEN, BLUE, YELLOW, PINK, WHITE)FXXSubstantially EquivalentCreative Contract (M) Sdn Bhdaccessdata.fda.gov

Compare with other makers

Updated March 5, 2003. 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.