Data / Medical devices / Cover, Shoe, Operating-Room / Cambodia
FDA-registered makers of Cover, Shoe, Operating-Room in Cambodia: 8 establishments
8 establishments in Cambodia are registered with the FDA to make Cover, Shoe, Operating-Room (product code FXP). 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
- Cover, Shoe, Operating-Room
- Product code
- FXP
- Country
- Cambodia
Makers of Cover, Shoe, Operating-Room in Cambodia
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Andersen Industries Co., Ltd. | Angsnoul District Kandal, Cambodia | Contract manufacturer, Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Cam A P I Medical Co., Ltd. | Angsnuol District Kandal, Cambodia | Contract manufacturer, Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Copious (cambodia) International Inc. | Takeo, Cambodia | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Fullmed Industrial Co.,ltd. | Samrong Tong district Kampong Speu, Cambodia | Contract manufacturer, Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Medtecs (cambodia) Corp. Limited | Srok Kampong Siem Kampong Cham, Cambodia | Contract manufacturer, Exporter to the US | 0 | 0 | 0 | 0 | api.fda.gov | |
| Paneffort (cambodia) Garment Co., Ltd. | Pot Sar Ward, Bati District Takeo, Cambodia | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Samaritan Textile (cambodia) Co., Ltd. | Phnom Penh, Cambodia | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Suning Junqi Medical Hygiene Products (cambodia) Co., Ltd. | Kampong Soam Preah Sihanouk, Cambodia | Contract manufacturer, 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.