Data / Medical devices / Cylinder, Compressed Gas, And Valve
Cylinder, Compressed Gas, And Valve (ECX): 13 FDA-registered makers in 4 countries
13 establishments in 4 countries are registered with the FDA to make Cylinder, Compressed Gas, And Valve (product code ECX, Class 1, 21 CFR 868.2700). 2 of them have a 510(k) clearance or PMA approval on file and 0 have a recall event. The FDA has issued 13 510(k) clearances under this code, the latest on April 13, 2017, and lists 5 recall events (0 Class I). FDA data exported November 2, 2026.
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- Product code
- ECX
- Device class
- 1
- Regulation
- 868.2700
- Medical specialty
- Anesthesiology
Makers by country
| Country | Makers |
|---|---|
| China | 8 |
| United States | 3 |
| Luxembourg | 1 |
| India | 1 |
Makers of Cylinder, Compressed Gas, And Valve
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 |
|---|---|---|---|---|---|---|---|---|
| Airgas USA | Houston, TX, United States | Specification developer | 3 | April 13, 2017 | 0 | 0 | 0 | api.fda.gov |
| Control Devices - Carr Lane | Saint Louis, MO, United States | Manufacturer, Remanufacturer | 1 | November 18, 2016 | 0 | 0 | 0 | api.fda.gov |
| Ceodeux S.A. | LINTGEN Luxembourg, Luxembourg | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Danyang Airtech Co.,ltd | danyang Jiangsu, China | Contract manufacturer, Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Danyang Xinya Valve Co., Ltd. | Danyang Jiangsu, China | Contract manufacturer, 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 | |
| Hangzhou Rollmed Co.,ltd. | Hangzhou Zhejiang, China | Contract manufacturer, Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Jiangsu Jumao X-Care Medical Equipment Co., Ltd | Danyang Jiangsu, China | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Jiangsu Mcare Medical Co.,ltd. | Danyang Jiangsu, China | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Life Corporation | Orlando, FL, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Shanghai Tianhai Composite Cylinders Co., Ltd. | Shanghai, China | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Yuyao Jiahua Medical Appliance, Co., Ltd. | Yuyao Zhejiang, China | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| ZJG Royaltrust Med Co., Ltd. | Zhangjiagang City Jiangsu, China | Contract manufacturer, Exporter to the US, Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov |
Updated April 13, 2017. 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.