Data / Medical devices / Device, Paste-On For Incontinence, Non-Sterile / United States
FDA-registered makers of Device, Paste-On For Incontinence, Non-Sterile in the United States: 9 establishments
9 establishments in the United States are registered with the FDA to make Device, Paste-On For Incontinence, Non-Sterile (product code NOA). 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
- Device, Paste-On For Incontinence, Non-Sterile
- Product code
- NOA
- Country
- United States
Makers of Device, Paste-On For Incontinence, Non-Sterile in the United States
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| ARGENTUM MEDICAL, LLC dba Bravida Medical | Geneva, IL, United States | Manufacturer | 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 | |
| Comfortland International, LLC | Mebane, NC, 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 | |
| Hollister Incorporated | Stuarts Draft, VA, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Medbio, LLC. | Grand Rapids, MI, United States | Contract 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 | |
| Sbe Medical Inc. | Comstock Park, MI, United States | Complaint file establishment, Repackager or relabeler, Specification developer | 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.