Data / Medical devices / Pack, Hot Or Cold, Disposable / Vietnam
FDA-registered makers of Pack, Hot Or Cold, Disposable in Vietnam: 5 establishments
5 establishments in Vietnam are registered with the FDA to make Pack, Hot Or Cold, Disposable (product code IMD). 1 has a 510(k) clearance or PMA approval on file and 0 have a recall event. FDA data exported November 3, 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.
- Device
- Pack, Hot Or Cold, Disposable
- Product code
- IMD
- Country
- Vietnam
Makers of Pack, Hot Or Cold, Disposable in Vietnam
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Rapid Aid Vietnam Co., Ltd | An Quang Commune Hai Phong, Vietnam | Complaint file establishment, Contract manufacturer, Exporter to the US, Foreign private label distributor, Manufacturer | 1 | July 24, 2017 | 0 | 0 | 0 | api.fda.gov |
| Actlife Technology Co., Ltd - Thanh Hoa Branch | Trung Chinh Commune Thanh Hoa, Vietnam | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Intco Medical Technology Viet Nam Company Limited | Dong Mai Ward Quang Ninh, Vietnam | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Koolcare Medical Equipment (vietnam) Company Limited | Ho Chi Minh City, Vietnam | Contract manufacturer, Exporter to the US, Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Yong Yi Viet Nam Co.,ltd | Duc Hoa Commune Tay Ninh, Vietnam | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov |
Updated November 3, 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.