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Sign in to claim this brandTradex Holdings LLC
US
Last updated May 24, 2026
What Tradex Holdings LLC makes
Tradex Holdings LLC manufactures nitrile examination and treatment gloves, including non-powdered, non-antimicrobial versions and sterile variants. These products are designed for medical, dental, and laboratory use to provide barrier protection during procedures.
The company’s portfolio is classified under FDA’s Class I medical devices and is listed in the FDA’s Unique Device Identifier (UDI) database. The manufacturer operates from 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 Tradex Holdings LLC manufacture?
Tradex Holdings LLC specializes in nitrile examination and treatment gloves. These include both non-powdered, non-antimicrobial gloves and sterile variants, which are primarily used in medical, dental, and laboratory settings to provide barrier protection during procedures.
Where is Tradex Holdings LLC based?
Tradex Holdings LLC is based in the United States. The company’s headquarters and operations are located within the country, though specific regional offices or manufacturing sites are not detailed in the available information.
Which regulatory registries list Tradex Holdings LLC’s devices?
Tradex Holdings LLC’s devices are listed in the FDA’s Unique Device Identifier (UDI) database. This registry ensures traceability and transparency for Class I medical devices, including the company’s nitrile gloves, by assigning a unique identifier to each product.
How are Tradex Holdings LLC’s devices classified by regulatory authorities?
Tradex Holdings LLC’s nitrile examination and treatment gloves fall under the FDA’s Class I medical device classification. This classification applies to low-risk devices that pose minimal potential harm to users, such as single-use gloves, which typically require less stringent regulatory oversight compared to higher-risk categories.
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
- 118875127
Catalogue (16)
| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Ambitex | LMD240 | FDA UDI | Class I | Unknown |
| Ambitex | NXL200G | FDA UDI | Class I | Active |
| Ambitex | NMD200G | FDA UDI | Class I | Active |
| Ambitex | LXS240 | FDA UDI | Class I | Unknown |
| Ambitex | NLG200G | FDA UDI | Class I | Active |
| Ambitex | LLG620 | FDA UDI | Class I | Unknown |
| Ambitex | LSM240 | FDA UDI | Class I | Unknown |
| Ambitex | GDN22024 | FDA UDI | Class I | Unknown |
| Ambitex | LSM620 | FDA UDI | Class I | Unknown |
| Ambitex | 33470-4 | FDA UDI | Class I | Active |
| Ambitex | LMD620 | FDA UDI | Class I | Unknown |
| Ambitex | LLG240 | FDA UDI | Class I | Unknown |
| Ambitex | LXL620 | FDA UDI | Class I | Unknown |
| Ambitex | LLG800 | FDA UDI | Class I | Unknown |
| Ambitex | NSM200G | FDA UDI | Class I | Active |
| Ambitex | LXL240 | FDA UDI | Class I | Unknown |
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