Data / Medical devices / Tampon, Menstrual, Scented, Scented-Deodorized
Tampon, Menstrual, Scented, Scented-Deodorized (HIL): 6 FDA-registered makers in 3 countries
6 establishments in 3 countries are registered with the FDA to make Tampon, Menstrual, Scented, Scented-Deodorized (product code HIL, Class 2, 21 CFR 884.5460). 6 of them have a 510(k) clearance or PMA approval on file and 0 have a recall event. The FDA has issued 84 510(k) clearances under this code, the latest on April 10, 2014, and lists 0 recall events (0 Class I). FDA data exported November 2, 2026.
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- Product code
- HIL
- Device class
- 2
- Regulation
- 884.5460
- Medical specialty
- Obstetrics/Gynecology
Makers by country
| Country | Makers |
|---|---|
| United States | 4 |
| Israel | 1 |
| Hungary | 1 |
Makers of Tampon, Menstrual, Scented, Scented-Deodorized
Registered establishments that manufacture, contract manufacture, remanufacture, reprocess or own the specification of this device, with the 510(k) clearances, PMA approvals and recalls the FDA files under each. Best documented first.
| 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 | 9 | October 9, 2013 | 0 | 0 | 0 | api.fda.gov |
| Albaad Massuot Yitzhak - FEM IL | CAESAREA Haifa, Israel | Manufacturer, Repackager or relabeler | 1 | November 23, 2004 | 0 | 0 | 0 | api.fda.gov |
| Hyginett Hungarian American Co. For The Production | CSOMOR Pest, Hungary | Manufacturer | 1 | June 27, 2008 | 0 | 0 | 0 | api.fda.gov |
| Pixie, Inc. | New York, NY, United States | Specification developer | 1 | November 23, 2004 | 0 | 0 | 0 | api.fda.gov |
| Procter & Gamble Co. | Cincinnati, OH, United States | Complaint file establishment, Specification developer | 1 | June 27, 2008 | 0 | 0 | 0 | api.fda.gov |
| Tambrands Inc. | Auburn, ME, United States | Manufacturer | 1 | June 27, 2008 | 0 | 0 | 0 | api.fda.gov |
Updated April 10, 2014. 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.