Data / Medical devices / Tourniquet, Nonpneumatic / Malaysia
FDA-registered makers of Tourniquet, Nonpneumatic in Malaysia: 5 establishments
5 establishments in Malaysia are registered with the FDA to make Tourniquet, Nonpneumatic (product code GAX). 0 have a 510(k) clearance or PMA approval on file and 0 have a recall event. FDA data exported November 2, 2026.
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- Device
- Tourniquet, Nonpneumatic
- Product code
- GAX
- Country
- Malaysia
Makers of Tourniquet, Nonpneumatic in Malaysia
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Innovate Medical Malaysia, Sdn. Bhd. | Shah Alam Selangor, Malaysia | Contract manufacturer, Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Itl Asia Pacific Sdn Bhd | Batu Gajah Perak, Malaysia | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Texstrip Manufacturing SDN.BHD. | Darul Ehsan Selangor, Malaysia | Contract manufacturer, Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| The Hygenic Corporation | Batu Gajah Perak, Malaysia | Contract manufacturer, Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| United Dragons Sdn. Bhd. | Melaka, Malaysia | Contract manufacturer | 0 | 0 | 0 | 0 | api.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.