Data / Medical devices / Collector, Urine, Powered, Non Indwelling Catheter / United States
FDA-registered makers of Collector, Urine, Powered, Non Indwelling Catheter in the United States: 13 establishments
13 establishments in the United States are registered with the FDA to make Collector, Urine, Powered, Non Indwelling Catheter (product code NZU). 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
- Collector, Urine, Powered, Non Indwelling Catheter
- Product code
- NZU
- Country
- United States
Makers of Collector, Urine, Powered, Non Indwelling Catheter in the United States
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Alpep LLC | Orange, CA, United States | Manufacturer, Repackager or relabeler | 0 | 0 | 0 | 0 | api.fda.gov | |
| Boehringer Laboratories, LLC | Phoenixville, PA, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| C.R. Bard, Inc. | Covington, GA, United States | Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| CM Technologies, Inc. | Carrollton, TX, United States | Complaint file establishment, Manufacturer, Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Compactcath, Inc | Palo Alto, CA, United States | Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Dielectrics, Inc. | Chicopee, MA, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Dymax, Corp. | Zelienople, PA, United States | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Forg Medical, Inc. | Seattle, WA, United States | Complaint file establishment, Repackager or relabeler, Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| HR PHARMACEUTICALS, INC d/b/a HR HealthCare | York, PA, United States | Complaint file establishment, Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| MEDLINE INDUSTRIES, LP - Northfield | Northfield, IL, United States | Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Omni Measurement Systems, Inc. | Colchester, VT, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Sage Products LLC | Cary, IL, United States | Manufacturer, Specification developer | 0 | 0 | 1 | 0 | api.fda.gov | |
| W.H.P.M., Inc. | Irwindale, CA, United States | Contract 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.