Data / Medical devices / Portable Liquid Oxygen Unit Stand
Portable Liquid Oxygen Unit Stand (PCM): 16 FDA-registered makers in 5 countries
16 establishments in 5 countries are registered with the FDA to make Portable Liquid Oxygen Unit Stand (product code PCM, Class 1, 21 CFR 890.5050). 0 of them have a 510(k) clearance or PMA approval on file and 0 have a recall event. The FDA has issued 1 510(k) clearance under this code, the latest on December 27, 2012, and lists 0 recall events (0 Class I). 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.
- Product code
- PCM
- Device class
- 1
- Regulation
- 890.5050
- Medical specialty
- Physical Medicine
Makers by country
| Country | Makers |
|---|---|
| China | 11 |
| India | 2 |
| Taiwan | 1 |
| Israel | 1 |
| United States | 1 |
Makers of Portable Liquid Oxygen Unit Stand
Registered establishments that manufacture, contract manufacture, remanufacture, reprocess or own the specification of this device, with the 510(k) clearances, PMA approvals and recalls the FDA files under each. Best documented first.
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Apex Health Care MFG., Inc. | Min Hsiung Shiang Chiayi(County), Taiwan | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Bliss Health Products Co., Ltd. | Zhongshan City Guangdong, China | Contract manufacturer, Exporter to the US, Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Cit (foshan)technology Co. Ltd. | FOSHAN Guangdong, China | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Danyang Huayi Medical Supply & Equipment Co, Ltd | DANYANG Jiangsu, China | Contract manufacturer, Exporter to the US, Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Flight Medical Innovations Ltd. | PETACH TIKVA Central, Israel | Exporter to the US, Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Greens Surgicals Private Limited | Vadodara Gujarat, India | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Guangzhou Konmison Technology Co., Ltd. | Guangzhou Guangdong, China | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Heuer International (A division of GST Corporation Limited) | NOIDA Uttar Pradesh, India | Foreign private label distributor, Manufacturer, Repackager or relabeler | 0 | 0 | 0 | 0 | api.fda.gov | |
| Jiangyin Newrise Medical Equipment Co.,ltd | JiangYin Jiangsu, China | Contract manufacturer, Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Jiangyin Huashi Medical Equipment Co.,Ltd | Jiangyin City Jiangsu, China | Exporter to the US, Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Qingdao Enmei Hai Leather Products Co.,ltd | QINGDAO Shandong, China | Exporter to the US, Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| RKS Est(shanghai) Co.. Ltd | Shanghai, China | Contract manufacturer, Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Shenyang Henyi Enterprise Co., Ltd | Shenyang Liaoning, China | Contract manufacturer, Exporter to the US, Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Taicang Jingquan Metal Products Co., Ltd | Taicang Jiangsu, China | Contract manufacturer, Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Tianjin Tairuibosi Medical Appliance Co., Ltd. | Tianjin, China | Exporter to the US, Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Telesair, Inc. | Irvine, CA, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov |
Updated December 27, 2012. 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.