Data / Medical devices / Uroflowmeter / United States
FDA-registered makers of Uroflowmeter in the United States: 15 establishments
15 establishments in the United States are registered with the FDA to make Uroflowmeter (product code EXY). 0 have a 510(k) clearance or PMA approval on file and 1 has a recall event. FDA data exported November 2, 2026.
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- Device
- Uroflowmeter
- Product code
- EXY
- Country
- United States
Makers of Uroflowmeter in the United States
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Adm Tronics Unltd, Inc. | Northvale, NJ, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Blur Product Development | Cary, NC, United States | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Bright Uro, Inc. | Irvine, CA, United States | Complaint file establishment, Manufacturer, Repackager or relabeler, Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Cal-Comp Usa | Carlsbad, CA, United States | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Caretech Human Inc | Ithaca, NY, United States | Complaint file establishment, Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Emano Metrics, Inc. | Eugene, OR, United States | Manufacturer | 0 | 0 | 1 | 0 | api.fda.gov | |
| I/O Urology Corporation | Knoxville, TN, United States | Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Laborie Medical Technologies Corp. | Portsmouth, NH, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Nextern | Maple Grove, MN, United States | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Potrero Medical, Inc. | Hayward, CA, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| SRS Medical | Chelmsford, MA, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Tecan Cdmo Solutions MH, Corp. | Morgan Hill, CA, United States | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| The Prometheus Group | Dover, NH, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Tensentric, LLC | Louisville, CO, United States | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Verathon Inc. | Bothell, WA, 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.