Data / Medical devices / Table, Physical Therapy, Multi Function
Table, Physical Therapy, Multi Function (JFB): 6 FDA-registered makers in 3 countries
6 establishments in 3 countries are registered with the FDA to make Table, Physical Therapy, Multi Function (product code JFB, Class 2, 21 CFR 890.5880). 6 of them have a 510(k) clearance or PMA approval on file and 0 have a recall event. The FDA has issued 66 510(k) clearances under this code, the latest on July 11, 2025, and lists 0 recall events (0 Class I). FDA data exported November 2, 2026.
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- Product code
- JFB
- Device class
- 2
- Regulation
- 890.5880
- Medical specialty
- Physical Medicine
Makers by country
| Country | Makers |
|---|---|
| United States | 3 |
| South Korea | 2 |
| Argentina | 1 |
Makers of Table, Physical Therapy, Multi Function
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 |
|---|---|---|---|---|---|---|---|---|
| Ceragem Co., Ltd. | Cheonan-si, Seobuk-gu Chungnam, South Korea | Manufacturer | 7 | July 11, 2025 | 0 | 0 | 0 | api.fda.gov |
| Nuga Medical Co Ltd | Wonju Gangwon, South Korea | Manufacturer | 2 | September 12, 2024 | 0 | 0 | 0 | api.fda.gov |
| Hill Laboratories | Frazer, PA, United States | Manufacturer | 1 | December 14, 2006 | 0 | 0 | 0 | api.fda.gov |
| Marzzan Lucas Jorge | Rosario Santa Fe, Argentina | Manufacturer | 1 | January 31, 2025 | 0 | 0 | 0 | api.fda.gov |
| TJN Manufacturing,inc. | Davenport, IA, United States | Manufacturer | 1 | May 26, 1993 | 0 | 0 | 0 | api.fda.gov |
| Williams Healthcare Systems, LLC. | Elgin, IL, United States | Manufacturer | 1 | February 2, 1994 | 0 | 0 | 0 | api.fda.gov |
Updated July 11, 2025. 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.