Data / Medical devices / Chair, Posture, For Cardiac And Pulmonary Treatment
Chair, Posture, For Cardiac And Pulmonary Treatment (BYN): 5 FDA-registered makers in 4 countries
5 establishments in 4 countries are registered with the FDA to make Chair, Posture, For Cardiac And Pulmonary Treatment (product code BYN, Class 1, 21 CFR 868.5365). 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 February 11, 1988, and lists 0 recall events (0 Class I). FDA data exported November 2, 2026.
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- Product code
- BYN
- Device class
- 1
- Regulation
- 868.5365
- Medical specialty
- Anesthesiology
Makers by country
| Country | Makers |
|---|---|
| United States | 2 |
| Mexico | 1 |
| India | 1 |
| China | 1 |
Makers of Chair, Posture, For Cardiac And Pulmonary Treatment
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 |
|---|---|---|---|---|---|---|---|---|
| Joerns Healthcare | Charlotte, NC, United States | Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Joerns Healthcare | Arlington, TX, United States | Complaint file establishment, Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Joerns Healthcare Matamoros | H. Matamoros, Tamaulipas Mexico, Mexico | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| SPM Medicare Pvt, Ltd. | NOIDA Uttar Pradesh, India | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Yasee Biomedical Inc | QINGDAO Shandong, China | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov |
Updated February 11, 1988. 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.