Data / Medical devices / United States / Tambrands Inc.
Tambrands Inc.: FDA-registered device maker in Auburn, ME, United States, 4 510(k) clearances
Tambrands Inc. is registered with the FDA (registration 1219109) in Auburn, ME, United States. It lists 2 device types. The FDA files 4 510(k) clearances under its listings, the newest dated January 9, 2014. Registered through 2027. FDA data exported November 2, 2026.
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- FDA registration number
- 1219109
- Address
- 2879 Hotel Rd, Auburn, ME, United States, 04210
- Owner or operator
- Procter & Gamble (9915005)
- Roles
- Manufacturer
- First device listed
- April 4, 2012
- Registered through
- 2027
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Tampon, Menstrual, Scented, Scented-Deodorized | HIL | 2 | Manufacturer | accessdata.fda.gov |
| Tampon, Menstrual, Unscented | HEB | 2 | Manufacturer | accessdata.fda.gov |
510(k) clearances
The 510(k) numbers this establishment lists, with the FDA decision on each. The applicant is the company that holds the clearance.
| Decided | 510(k) number | Device | Product code | Decision | Applicant | Source |
|---|---|---|---|---|---|---|
| January 9, 2014 | K133244 | TAMPAX M PLASTIC TAMPONS, UNSCENTED | HEB | Substantially Equivalent | The Procter & Gamble Company | accessdata.fda.gov |
| June 2, 2011 | K110669 | TAMPAX C PLASTIC TAMPONS, UNSCENTED | HEB | Substantially Equivalent | The Procter & Gamble Co. | accessdata.fda.gov |
| June 27, 2008 | K081555 | TAMPAX PEARL PLASTIC APPLICATOR TAMPONS, SCENTED AND UNSCENTED | HIL | Substantially Equivalent | Procter & Gamble Co. | accessdata.fda.gov |
| August 1, 2006 | K061486 | TAMPAX TAMPONS - (LIGHT,REGULAR,SUPER AND SUPER PLUS ABSORBENCIES) | HEB | Substantially Equivalent | Procter & Gamble Co. | accessdata.fda.gov |
Compare with other makers
- All makers of Tampon, Menstrual, Unscented
- All makers of Tampon, Menstrual, Scented, Scented-Deodorized
Updated January 9, 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.