Data / Medical devices / Yoke Assembly, Medical Gas
Yoke Assembly, Medical Gas (CAM): 15 FDA-registered makers in 5 countries
15 establishments in 5 countries are registered with the FDA to make Yoke Assembly, Medical Gas (product code CAM, Class 1, 21 CFR 868.6885). 0 of them have a 510(k) clearance or PMA approval on file and 0 have a recall event. The FDA has issued 8 510(k) clearances under this code, the latest on March 11, 1994, and lists 0 recall events (0 Class I). FDA data exported November 2, 2026.
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- Product code
- CAM
- Device class
- 1
- Regulation
- 868.6885
- Medical specialty
- Anesthesiology
Makers by country
| Country | Makers |
|---|---|
| United States | 8 |
| China | 3 |
| Taiwan | 2 |
| Germany | 1 |
| Mexico | 1 |
Makers of Yoke Assembly, Medical Gas
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 |
|---|---|---|---|---|---|---|---|---|
| Accutron, Inc. | Phoenix, AZ, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Allied Medical LLC | Earth City, MO, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Bay Corporation | Westlake, OH, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Belmed, Inc. | Red Lion, PA, United States | Complaint file establishment, Contract manufacturer, Contract sterilizer, Manufacturer, Manufacturer for export, Remanufacturer, Repackager or relabeler, Reprocessor, Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Danyang Xinya Valve Co., Ltd. | Danyang Jiangsu, China | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Doner Industries, Inc. | Rogers, AR, United States | Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Gentec (shanghai) Corporation | Shanghai, China | Exporter to the US, Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Ningbo Chibanda Imp &exp Co, Ltd | Ningbo Zhejiang, China | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Richard Wolf GMBH | KNITTLINGEN Baden-Wurttemberg, Germany | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| SEI Medical S.A. de C.V. | Juarez Chihuahua, Mexico | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Soleetech Corporation | Lujhou Taipei, Taiwan | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Sun May Industrial Co., Ltd. | Pan Chiao City Taipei, Taiwan | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Superior Products, LLC | Brooklyn, OH, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| TOUCHPOINT MEDICAL, Inc. | Odessa, FL, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Western Enterprises, Inc. | Westlake, OH, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov |
Updated March 11, 1994. 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.