Data / Medical devices / Tampon, Menstrual, Unscented / United States
FDA-registered makers of Tampon, Menstrual, Unscented in the United States: 14 establishments
14 establishments in the United States are registered with the FDA to make Tampon, Menstrual, Unscented (product code HEB). 11 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
- Tampon, Menstrual, Unscented
- Product code
- HEB
- Country
- United States
Makers of Tampon, Menstrual, Unscented in the United States
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Essity HMS North America Inc. | Dover, DE, United States | Complaint file establishment, Manufacturer, Repackager or relabeler, Specification developer | 5 | May 30, 2018 | 0 | 0 | 0 | api.fda.gov |
| Procter & Gamble Co. | Cincinnati, OH, United States | Complaint file establishment, Specification developer | 4 | January 9, 2014 | 0 | 0 | 0 | api.fda.gov |
| Rael, Inc. | Buena Park, CA, United States | Repackager or relabeler, Specification developer | 4 | October 7, 2019 | 0 | 0 | 0 | api.fda.gov |
| Kimberly-Clark Corporation | Neenah, WI, United States | Complaint file establishment, Repackager or relabeler, Specification developer | 3 | August 13, 2025 | 0 | 1 | 0 | api.fda.gov |
| Tambrands Inc. | Auburn, ME, United States | Manufacturer | 3 | January 9, 2014 | 0 | 0 | 0 | api.fda.gov |
| Pixie Cup LLC | Walnut Shade, MO, United States | Complaint file establishment, Specification developer | 2 | August 13, 2025 | 0 | 0 | 0 | api.fda.gov |
| TPC Inc. | New York, NY, United States | Specification developer | 2 | August 13, 2025 | 0 | 0 | 0 | api.fda.gov |
| Best Logistics | South Brunswick, NJ, United States | Specification developer | 1 | April 29, 2009 | 0 | 0 | 0 | api.fda.gov |
| Liviwell Inc | Mountain Lakes, NJ, United States | Complaint file establishment, Specification developer | 1 | March 20, 2026 | 0 | 0 | 0 | api.fda.gov |
| Pixie, Inc. | New York, NY, United States | Specification developer | 1 | December 7, 2006 | 0 | 0 | 0 | api.fda.gov |
| Tampro Inc | San Francisco, CA, United States | Complaint file establishment, Specification developer | 1 | August 3, 2023 | 0 | 0 | 0 | api.fda.gov |
| R.K. Manufacturing | Danbury, CT, United States | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Reddrop Inc | Atlanta, GA, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Tampon Tribe Inc | Santa Monica, 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.