Data / Medical devices / Pad, Menstrual, Reusable / United States
FDA-registered makers of Pad, Menstrual, Reusable in the United States: 11 establishments
11 establishments in the United States are registered with the FDA to make Pad, Menstrual, Reusable (product code NUQ). 0 have a 510(k) clearance or PMA approval on file and 0 have a recall event. FDA data exported November 2, 2026.
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- Device
- Pad, Menstrual, Reusable
- Product code
- NUQ
- Country
- United States
Makers of Pad, Menstrual, Reusable in the United States
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Adidas | Portland, OR, United States | Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Domino Pads | Floresville, TX, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Goat Union, LLC | Atlanta, GA, United States | Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| GladRags | Portland, OR, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Kimberly-Clark Corporation | Neenah, WI, United States | Complaint file establishment, Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Luci Daum Design LLC | Ashland, WI, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Mary and Bird, LLC | Ogden, UT, United States | Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Pixie Cup LLC | Walnut Shade, MO, United States | Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Procter & Gamble Co. | Cincinnati, OH, United States | Complaint file establishment, Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Saalt, LLC | Boise, ID, United States | Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Tampon Tribe Inc | Santa Monica, CA, United States | Repackager or relabeler, Specification developer | 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.