Data / Medical devices / Bag, Urine Collection, Leg, For External Use, Non-Sterile / United States
FDA-registered makers of Bag, Urine Collection, Leg, For External Use, Non-Sterile in the United States: 15 establishments
15 establishments in the United States are registered with the FDA to make Bag, Urine Collection, Leg, For External Use, Non-Sterile (product code NNW). 0 have a 510(k) clearance or PMA approval on file and 0 have a recall event. FDA data exported November 3, 2026.
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- Device
- Bag, Urine Collection, Leg, For External Use, Non-Sterile
- Product code
- NNW
- Country
- United States
Makers of Bag, Urine Collection, Leg, For External Use, Non-Sterile in the United States
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Acosta Medical Group Inc. | Houston, TX, United States | Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Alimed, LLC | Dedham, MA, United States | Manufacturer, Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Ansell Healthcare Products LLC | Reno, NV, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Alltrista Plastics LLC | Reedsville, PA, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Ansell Sandel Medical Solutions LLC | Chatsworth, CA, United States | Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Beauxregard Industries | Sarasota, FL, United States | Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| C.R. Bard, Inc. | Covington, GA, United States | Contract sterilizer, Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| David Scott Company. | Franklin, MA, United States | Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Greystone Medical, LLC | Waterford, MI, United States | Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Hill-Rom, Inc. | Batesville, IN, United States | Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Hollister Incorporated | Libertyville, IL, United States | Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Kova International Inc | Garden Grove, CA, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Skil-Care Corp. | New Rochelle, NY, United States | Manufacturer, Repackager or relabeler | 0 | 0 | 0 | 0 | api.fda.gov | |
| Tidi Products, LLC | Neenah, WI, United States | Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Urocare Products, Inc. | Pomona, CA, 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.