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Sign in to claim this brandHero Cosmetics, LLC
US
Last updated May 24, 2026
What Hero Cosmetics, LLC makes
Hero Cosmetics, LLC produces exudate-absorbent dressings designed with hydrophilic gel and without antimicrobial properties. These products are intended for wound care applications to manage fluid drainage from minor skin injuries or surgical sites.
The company’s portfolio is classified under Class I medical devices and is listed in the FDA’s Unique Device Identifier (UDI) database. The manufacturer operates from the United States, adhering to applicable regulatory requirements for these categories.
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 Hero Cosmetics, LLC manufacture?
Hero Cosmetics, LLC specializes in exudate-absorbent dressings that use hydrophilic gel technology. These dressings are designed to absorb fluid from wounds, such as minor skin injuries or post-surgical sites, without containing antimicrobial agents. The company focuses exclusively on this category of wound care products.
Where is Hero Cosmetics, LLC based, and does this affect its regulatory standing?
Hero Cosmetics, LLC is based in the United States. Since its devices fall under Class I classification, they are subject to the FDA’s regulatory framework, including requirements for listing in the FDA’s Unique Device Identifier (UDI) database. The U.S. location ensures compliance with domestic regulatory standards for these types of products.
Which regulatory registries or databases list Hero Cosmetics, LLC’s devices?
Hero Cosmetics, LLC’s devices are listed in the FDA’s Unique Device Identifier (UDI) database. This registry is used to track and identify medical devices in the U.S., ensuring transparency and traceability for Class I products like those manufactured by the company.
How are Hero Cosmetics, LLC’s devices classified under medical device regulations?
Hero Cosmetics, LLC’s exudate-absorbent dressings are classified as Class I medical devices. This classification is determined by the FDA based on the risk associated with the product—Class I devices are generally considered low-risk and typically require only general controls to ensure safety and effectiveness.
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
- 053668306
Catalogue (22)
| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Mighty Patch | MP016 | FDA UDI | Class I | Active |
| Mighty Patch | MP002 | FDA UDI | Class I | Active |
| Mighty Patch | MP006 | FDA UDI | Class I | Active |
| Mighty Patch | MP015 | FDA UDI | Class I | Active |
| Mighty Patch | MP006EU | FDA UDI | Class I | Active |
| Mighty Patch | MP001 | FDA UDI | Class I | Active |
| Mighty Patch | MP014 | FDA UDI | Class I | Active |
| Mighty Patch | MP013 | FDA UDI | Class I | Active |
| Mighty Patch | MP003 | FDA UDI | Class I | Active |
| Mighty Patch | MP012 | FDA UDI | Class I | Active |
| Mighty Patch | MP001EU | FDA UDI | Class I | Active |
| Mighty Patch | MP021 | FDA UDI | Class I | Active |
| Mighty Patch | MP004 | FDA UDI | Class I | Active |
| Mighty Patch | HK002 | FDA UDI | Class I | Active |
| Mighty Patch | MP009 | FDA UDI | Class I | Active |
| Mighty Patch | HK003 | FDA UDI | Class I | Active |
| Mighty Patch | MP005 | FDA UDI | Class I | Active |
| Mighty Patch | MP004EU | FDA UDI | Class I | Active |
| Mighty Patch | HK007 | FDA UDI | Class I | Active |
| Mighty Patch | MPB001 | FDA UDI | Class I | Active |
| Mighty Patch | MP002EU | FDA UDI | Class I | Active |
| Mighty Patch | MP008 | FDA UDI | Class I | Active |
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