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Sign in to claim this brandEDGEWELL PERSONAL CARE BRANDS, LLC
US
Last updated May 23, 2026
What EDGEWELL PERSONAL CARE BRANDS, LLC makes
The company manufactures menstrual hygiene products, including unscented and scented menstrual tampons and pads. These devices are designed for disposable use during menstruation and are marketed under multiple brand names.
The portfolio includes devices classified as Class I and Class II under FDA regulations, with all products listed in the FDA’s Unique Device Identifier (UDI) database. The company is based in the United States.
Written from this company's registered devices by an AI model, and not verified by a human reviewer.
Frequently asked questions
What types of medical devices does Edgewell Personal Care Brands, LLC manufacture?
Edgewell Personal Care Brands, LLC manufactures menstrual hygiene products, specifically disposable menstrual tampons and pads. These include both unscented and scented varieties, designed for use during menstruation. The devices fall under categories like menstrual tampons and menstrual pads, catering to consumer needs for comfort and discretion during their menstrual cycle.
Where is Edgewell Personal Care Brands, LLC based?
Edgewell Personal Care Brands, LLC is headquartered in the United States. This location is relevant for regulatory compliance and distribution, as the company operates within the FDA’s jurisdiction for its medical devices.
Which regulatory registries list Edgewell Personal Care Brands, LLC’s devices?
Edgewell Personal Care Brands, LLC’s devices are listed in the FDA’s Unique Device Identifier (UDI) database. The UDI system helps track and identify medical devices throughout their lifecycle, ensuring transparency and traceability for regulatory and market surveillance purposes.
How are Edgewell Personal Care Brands, LLC’s menstrual hygiene products classified under FDA regulations?
Edgewell Personal Care Brands, LLC’s menstrual hygiene products are classified as either Class I or Class II devices under FDA regulations. Class I devices generally pose minimal risk and may require general controls, while Class II devices involve a higher level of risk and may require special controls to ensure safety and effectiveness. The classification depends on factors like design complexity and potential health impact.
AI-generated from registry data and not verified by a human reviewer.
Information
- Country
- US
- Address
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- Website
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- Phone
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- PRRC Contact
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- EUDAMED SRN
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- FDA FEI Number
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- DUNS Number
- 151179769
Catalogue (162)
Page 4 of 4| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Playtex | 09923 | FDA UDI | Class II | Active |
| Playtex | 14110 | FDA UDI | Class II | Active |
| Playtex | 09846 | FDA UDI | Class II | Active |
| Playtex | 02691 | FDA UDI | Class II | Active |
| Carefree | 08447 | FDA UDI | Class I | Active |
| Stayfree | 07047 | FDA UDI | Class I | Active |
| Playtex | 07114 | FDA UDI | Class II | Active |
| Playtex | 08254 | FDA UDI | Class II | Active |
| Playtex | 03179 | FDA UDI | Class II | Active |
| Playtex | 08113 | FDA UDI | Class II | Active |
| Stayfree | 07027 | FDA UDI | Class I | Active |
| Playtex | 07112 | FDA UDI | Class II | Active |
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