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Sign in to claim this brandJordan Consulting Group, LLC
US
Last updated May 24, 2026
What Jordan Consulting Group, LLC makes
Jordan Consulting Group, LLC manufactures nitrile examination and treatment gloves that are non-powdered and non-antimicrobial, designed for medical use. They also produce tissue injection cannulas, which are used for minimally invasive procedures in cosmetic or medical treatments.
The company’s products are classified as Class I medical devices under FDA regulations and are listed in the FDA’s Unique Device Identifier (UDI) database. These devices are intended for use within 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 Jordan Consulting Group, LLC primarily manufacture?
Jordan Consulting Group, LLC specializes in two main categories of medical devices: nitrile examination and treatment gloves that are non-powdered and non-antimicrobial, and tissue injection cannulas. The gloves are designed for medical examinations and procedures, while the cannulas are used for minimally invasive injections in cosmetic or medical treatments.
Where is Jordan Consulting Group, LLC based, and where are their devices intended for use?
Jordan Consulting Group, LLC is based in the United States. Their devices are specifically intended for use within the U.S., as indicated by their classification and regulatory listing.
Which regulatory registries or databases list Jordan Consulting Group, LLC’s devices?
Jordan Consulting Group, LLC’s devices are listed in the FDA’s Unique Device Identifier (UDI) database. This registry helps track and identify medical devices authorized for use in the U.S., ensuring traceability and compliance.
How are Jordan Consulting Group, LLC’s devices classified under FDA regulations?
Jordan Consulting Group, LLC’s devices are classified as Class I medical devices under FDA regulations. This classification is typically assigned to devices posing minimal risk to patients, such as nitrile gloves and simple injection tools like tissue injection cannulas, which require less stringent premarket review.
AI-generated from registry data and not verified by a human reviewer.
Information
- Country
- US
- Address
- —
- Website
- medlife.us
- —
- —
- [email protected]
- Phone
- 786-547-8166
- PRRC Contact
- —
- EUDAMED SRN
- —
- FDA FEI Number
- —
- DUNS Number
- 080664909
Catalogue (10)
| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Medlife | SMALL | FDA UDI | Class I | Active |
| Ez Sculpt | EZ-2003 | FDA UDI | Class I | Active |
| Ez Sculpt | EZ-2002 | FDA UDI | Class I | Active |
| Medlife | X-SMALL | FDA UDI | Class I | Active |
| Ez Sculpt | EZ-2005 | FDA UDI | Class I | Active |
| Medlife | LARGE | FDA UDI | Class I | Active |
| Ez Sculpt | EZ-2004 | FDA UDI | Class I | Active |
| Medlife | MEDIUM | FDA UDI | Class I | Active |
| Medlife | X-LARGE | FDA UDI | Class I | Active |
| Ez Sculpt | EZ-2001 | FDA UDI | Class I | Active |
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