Data / Medical devices / Flowmeter, Tube, Thorpe, Back-Pressure Compensated / United States
FDA-registered makers of Flowmeter, Tube, Thorpe, Back-Pressure Compensated in the United States: 14 establishments
14 establishments in the United States are registered with the FDA to make Flowmeter, Tube, Thorpe, Back-Pressure Compensated (product code CAX). 1 has a 510(k) clearance or PMA approval on file and 1 has a recall event. FDA data exported November 3, 2026.
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- Device
- Flowmeter, Tube, Thorpe, Back-Pressure Compensated
- Product code
- CAX
- Country
- United States
Makers of Flowmeter, Tube, Thorpe, Back-Pressure Compensated in the United States
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Precision Fluidics Division Parker Hannifin Corp. | Hatfield, PA, United States | Manufacturer | 1 | June 10, 1993 | 0 | 1 | 0 | api.fda.gov |
| Allied Medical LLC | Earth City, MO, 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 | |
| Controls Corporation Of America | Virginia Beach, VA, United States | Manufacturer, Manufacturer for export | 0 | 0 | 0 | 0 | api.fda.gov | |
| Doner Industries, Inc. | Rogers, AR, United States | Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Fte Dynamics, LLC | Chino Hills, CA, United States | Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Mada Medical Products, Inc. | Carlstadt, NJ, United States | Manufacturer, Repackager or relabeler | 0 | 0 | 0 | 0 | api.fda.gov | |
| Nidek Medical Products, Inc. | Birmingham, AL, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Ohio Medical LLC | Gurnee, IL, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Precision Medical, Inc. | Northampton, PA, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Salaera, LLC d.b.a Maxtec | Salt Lake City, UT, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| SunMed Group Holdings, LLC | Grand Rapids, MI, United States | Complaint file establishment, Manufacturer, Repackager or relabeler | 0 | 0 | 0 | 0 | api.fda.gov | |
| The Harris Products Group | Gainesville, GA, 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 November 3, 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.