Data / Medical devices / Cambodia / Jumao Medical Equipment (cambodia) Co., Ltd.
Jumao Medical Equipment (cambodia) Co., Ltd.: FDA-registered device maker in Angk Snuol Kandal, Cambodia, 1 510(k) clearance
Jumao Medical Equipment (cambodia) Co., Ltd. is registered with the FDA (registration 3038189860) in Angk Snuol Kandal, Cambodia. It lists 3 device types. The FDA files 1 510(k) clearance under its listings, the newest dated December 22, 2025. Registered through 2026. FDA data exported November 3, 2026.
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- FDA registration number
- 3038189860
- Address
- No House/Building Number, National Road No. 51, Kdan Roy, Damnak Ampil, Angk Snuol Kandal, Cambodia, 12403
- Owner or operator
- JUMAO MEDICAL EQUIPMENT (CAMBODIA) CO., LTD. (10092947)
- Roles
- Contract manufacturer, Manufacturer
- First device listed
- March 10, 2025
- Registered through
- 2026
- Brand names listed
- Portable oxygen concentrator (JLO-190P), Rollator, Transport Chair,GVEXP19LTGY, Wheelchair,Transport chair
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Generator, Oxygen, Portable | CAW | 2 | Manufacturer | accessdata.fda.gov |
| Walker, Mechanical | ITJ | 1 | Manufacturer | accessdata.fda.gov |
| Wheelchair, Mechanical | IOR | 1 | Contract manufacturer | accessdata.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.
| Decided | 510(k) number | Device | Product code | Decision | Applicant | Source |
|---|---|---|---|---|---|---|
| December 22, 2025 | K252616 | Portable oxygen concentrator (JLO-190P) | CAW | Substantially Equivalent | Shenzhen Homed Medical Device Co., Ltd. | accessdata.fda.gov |
Compare with other makers
- All makers of Generator, Oxygen, Portable
- All makers of Wheelchair, Mechanical
- All makers of Walker, Mechanical
Updated December 22, 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.