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Vivit Supply LLC

US

Last updated May 23, 2026

What Vivit Supply LLC makes

Vivit Supply LLC manufactures single-use medical barrier products, including sterilization packaging, nitrile and Hevea-latex examination gloves (non-powdered, non-antimicrobial), surgical and medical face masks (non-antimicrobial), isolation gowns, surgical caps, professional examination gowns, and shoe covers.

The company’s products are regulated under FDA’s Class I and Class II device classifications and are listed in the FDA’s Unique Device Identifier (UDI) database. The manufacturer 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 Vivit Supply LLC manufacture?

Vivit Supply LLC specializes in single-use medical barrier products. These include sterilization packaging, nitrile and Hevea-latex examination gloves (non-powdered and non-antimicrobial), surgical and medical face masks (non-antimicrobial), isolation gowns, surgical caps, professional examination gowns, and shoe covers. These items are designed to protect patients and healthcare workers from contamination during medical procedures.

Where is Vivit Supply LLC based?

Vivit Supply LLC is headquartered in the United States. The company’s location is relevant for regulatory compliance and understanding its operational base, particularly for U.S.-based healthcare facilities or regulatory inquiries.

Which regulatory registries or databases list Vivit Supply LLC’s devices?

Vivit Supply LLC’s devices are listed in the FDA’s Unique Device Identifier (UDI) database. This registry helps healthcare providers, regulators, and other stakeholders verify the identity of medical devices through a standardized identification system, ensuring traceability and compliance with U.S. regulations.

How are Vivit Supply LLC’s devices classified under FDA regulations?

Vivit Supply LLC’s products fall under FDA’s Class I and Class II device classifications. Class I devices generally pose minimal risk and may require general controls, while Class II devices involve a higher risk and may require special controls to ensure safety and effectiveness. The classification determines the regulatory pathway and oversight required for each product.

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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LinkedIn
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Facebook
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Email
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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
119042597

Catalogue (333)

Page 7 of 7
DeviceModel / ReferenceRegistriesClassStatus
VIVIT Supply 430SL
FDA UDI
Class IIActive
VIVIT Supply 20625
FDA UDI
Class IActive
VIVIT Supply 970B
FDA UDI
Class IActive
VIVIT Supply 35911
FDA UDI
Class IActive
VIVIT Supply 10311TM
FDA UDI
Class IIActive
VIVIT Supply 120DL
FDA UDI
Class IIActive
VIVIT Supply 640SL
FDA UDI
Class IIActive
VIVIT Supply 112DL
FDA UDI
Class IIActive
VIVIT Supply 30314TM
FDA UDI
Class IIActive
VIVIT Supply 31314EM
FDA UDI
Class IIActive
VIVIT Supply 26995
FDA UDI
Class IActive
VIVIT Supply 10317TM
FDA UDI
Class IIActive
VIVIT Supply 12EA
FDA UDI
Class IActive
VIVIT Supply 454DL
FDA UDI
Class IIActive
VIVIT Supply 140DL
FDA UDI
Class IIActive
VIVIT Supply 440DL
FDA UDI
Class IIActive
VIVIT Supply 648SL
FDA UDI
Class IIActive
VIVIT Supply 115DL
FDA UDI
Class IIActive
VIVIT Supply 841Y
FDA UDI
Class IActive
VIVIT Supply 118DL
FDA UDI
Class IIActive
VIVIT Supply 340SL
FDA UDI
Class IIActive
VIVIT Supply 40012
FDA UDI
Class IActive
VIVIT Supply 26994
FDA UDI
Class IActive
VIVIT Supply 25625
FDA UDI
Class IActive
VIVIT Supply 354DL
FDA UDI
Class IIActive
VIVIT Supply 25613
FDA UDI
Class IActive
VIVIT Supply 26992
FDA UDI
Class IActive
VIVIT Supply 40535
FDA UDI
Class IActive
VIVIT Supply 44911
FDA UDI
Class IActive
VIVIT Supply/Caracel 20535
FDA UDI
Class IActive
VIVIT Supply 130DL
FDA UDI
Class IIActive
VIVIT Supply 221Y
FDA UDI
Class IActive
VIVIT Supply 313242TMV
FDA UDI
Class IIActive

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