Data / Medical devices / Table, Operating-Room, Mechanical
Table, Operating-Room, Mechanical (FWX): 13 FDA-registered makers in 8 countries
13 establishments in 8 countries are registered with the FDA to make Table, Operating-Room, Mechanical (product code FWX, Class 1, 21 CFR 878.4950). 0 of them have a 510(k) clearance or PMA approval on file and 0 have a recall event. The FDA has issued 3 510(k) clearances under this code, the latest on October 13, 1988, and lists 1 recall event (0 Class I). FDA data exported November 2, 2026.
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- Product code
- FWX
- Device class
- 1
- Regulation
- 878.4950
- Medical specialty
- General, Plastic Surgery
Makers by country
| Country | Makers |
|---|---|
| India | 3 |
| United States | 2 |
| Switzerland | 2 |
| China | 2 |
| Brazil | 1 |
| Taiwan | 1 |
| Germany | 1 |
| Indonesia | 1 |
Makers of Table, Operating-Room, Mechanical
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 |
|---|---|---|---|---|---|---|---|---|
| Apothecaries Sundries MFG Pvt Ltd | GURUGRAM Haryana, India | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Barrfab Industria Comercio Importacao De Equipamentos Hospit | Farroupilha Rio Grande do Sul, Brazil | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| BenQ Medical Technology Corporation | Taoyuan City, Taiwan | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Black Forest Medical GmbH | FREIBURG Baden-Wurttemberg, Germany | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Klyo Medical Systems Inc | Doral, FL, United States | Manufacturer, Repackager or relabeler | 0 | 0 | 0 | 0 | api.fda.gov | |
| Medacta International SA | Castel San Pietro Ticino, Switzerland | Repackager or relabeler, Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Medacta International SA | Rancate Ticino, Switzerland | Repackager or relabeler, Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Narang Medical, Ltd. | New Delhi, India | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| PT. Mega Andalan Kalasan | JOGYAKARTA Yogyakarta, Indonesia | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Shanghai Huifeng Medical Instrument Co., Ltd. | Shanghai, China | Contract manufacturer, Exporter to the US, Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Shanghai PAX Medical Instrument Co., Ltd. | Shanghai, China | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| United Poly Engineering Pvt. Ltd. | New Delhi, India | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Western Industries Corporation | Oklahoma City, OK, United States | Contract manufacturer, Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov |
Updated October 13, 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.