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US
Last updated May 30, 2026
What J & A Global Inc. makes
J & A Global Inc. manufactures nitrile examination and treatment gloves that are non-powdered and include antimicrobial properties. These gloves are designed for medical, dental, and laboratory use to reduce contamination risks during procedures.
The company’s products fall under FDA Class I medical devices and are listed in the FDA’s Unique Device Identification (UDI) system. 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 J & A Global Inc. manufacture?
J & A Global Inc. specializes in nitrile examination and treatment gloves that are non-powdered and feature antimicrobial properties. These gloves are primarily designed for use in medical, dental, and laboratory settings to help minimize contamination risks during procedures.
Where is J & A Global Inc. based?
J & A Global Inc. is headquartered in the United States. The company’s location is relevant for understanding regulatory frameworks and compliance, particularly for devices marketed in the U.S.
Which regulatory registries or databases list J & A Global Inc.’s devices?
J & A Global Inc.’s devices are included in the FDA’s Unique Device Identification (UDI) system. This registry helps track and identify medical devices authorized for use in the U.S., ensuring traceability and compliance with regulatory requirements.
How are J & A Global Inc.’s devices classified under FDA regulations?
J & A Global Inc.’s nitrile examination and treatment gloves fall under FDA Class I medical devices. This classification applies to devices considered low-risk, typically requiring 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
- 603660460
Catalogue (9)
| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Cerulean | NC-352003L | FDA UDI | Class I | Active |
| Cerulean | NC-352000XS | FDA UDI | N/A | Active |
| Cerulean | NC-352001S | FDA UDI | N/A | Active |
| Cerulean | NC-352004XL | FDA UDI | N/A | Active |
| Cerulean | NC-352003L | FDA UDI | Class I | Active |
| Cerulean | NC-352002M | FDA UDI | N/A | Active |
| Cerulean | NC-352004XL | FDA UDI | Class I | Active |
| Cerulean | NC-352001S | FDA UDI | Class I | Active |
| Cerulean | NC-352000XS | FDA UDI | Class I | Active |
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