Data / Medical devices / System, Pressure Measurement, Intermittent / United States
FDA-registered makers of System, Pressure Measurement, Intermittent in the United States: 11 establishments
11 establishments in the United States are registered with the FDA to make System, Pressure Measurement, Intermittent (product code JFC). 0 have a 510(k) clearance or PMA approval on file and 0 have a recall event. FDA data exported November 2, 2026.
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- Device
- System, Pressure Measurement, Intermittent
- Product code
- JFC
- Country
- United States
Makers of System, Pressure Measurement, Intermittent in the United States
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Blue Chip Medical Products, Inc. | Suffern, NY, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Clinical Image Retrieval Systems, Inc. | Franklin, NJ, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Djo, LLC | Carlsbad, CA, United States | Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Linus Health, Inc. | Boston, MA, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Med-Linket Corp | Alhambra, CA, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| ROHO, Inc. | Belleville, IL, United States | Complaint file establishment, Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Sportgait, Inc. | Wilmington, NC, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Tekscan, Inc. | Norwood, MA, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Vibetech Enterprises, LLC | Sheboygan, WI, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Wellsense, Inc. | Rochester Hills, MI, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| ZenoMetrics LLC | Peekskill, NY, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov |
Updated November 2, 2026. 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.