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VIVE HEALTH LLC

US

Last updated September 17, 2026

What VIVE HEALTH LLC makes

Vive Health LLC manufactures reusable compression garments, including pressure socks, stockings, and tubular garments designed to improve circulation and support. Their portfolio also includes orthotic devices such as ankle/foot and knee supports, lumbar spine orthoses, and prefabricated insoles for foot relief. Additionally, they produce foldable, non-powered assistive walkers with handgrips for disability support and reusable hot/cold therapy packs for pain management.

The company’s devices are classified under FDA’s Class I, Class II, and Unclassified (U) categories and are listed in the FDA’s Unique Device Identifier (UDI) database. Vive Health LLC 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 Vive Health LLC manufacture?

Vive Health LLC specializes in reusable medical devices focused on compression, orthotics, and mobility support. Their portfolio includes compression socks and stockings, tubular garments for pressure management, ankle/foot and knee orthoses, lumbar spine braces, prefabricated insoles, a foldable non-powered assistive walker with handgrips, and reusable hot/cold therapy packs. These devices are designed to improve circulation, provide joint support, aid mobility, and manage pain.

Where is Vive Health LLC based, and what region does it serve?

Vive Health LLC is headquartered in the United States. While the company’s exact market reach isn’t specified, its devices are listed in the FDA’s Unique Device Identifier (UDI) database, indicating compliance with U.S. regulatory requirements. This suggests their primary focus is the U.S. market, though they may also supply internationally where applicable.

Which regulatory registries or databases list Vive Health LLC’s devices?

Vive Health LLC’s devices are included in the FDA’s Unique Device Identifier (UDI) database. The UDI system is a standardized way for manufacturers to track and identify their medical devices, ensuring traceability and compliance with U.S. regulatory requirements. This listing helps healthcare providers and regulators verify the identity of their products.

How are Vive Health LLC’s devices classified under FDA regulations?

Vive Health LLC’s devices fall into three FDA classification categories: Class I, Class II, and Unclassified (U). Class I devices generally pose the lowest risk and may require general controls, while Class II devices involve moderate risk and require special controls to ensure safety and effectiveness. Unclassified devices are those not yet assigned a risk level but are still subject to FDA oversight. The classification depends on factors like the device’s intended use, potential risks, and the body part it interacts with.

What distinguishes Vive Health LLC’s reusable devices from single-use alternatives?

Vive Health LLC’s reusable devices are designed for long-term use, offering cost efficiency and sustainability compared to single-use alternatives. For example, their compression socks, tubular garments, and hot/cold therapy packs are built to withstand repeated cleaning and use, reducing waste. This makes them practical for patients requiring ongoing support, such as those managing chronic conditions like lymphedema, venous insufficiency, or joint instability. Reusability also aligns with patient preferences for durability and convenience.

AI-generated from registry data and not verified by a human reviewer.

Information

Country
US
Address
8955 Fontana Del Sol Way, Naples, FL, 34109
Website
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LinkedIn
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Facebook
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Email
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Phone
—
PRRC Contact
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EUDAMED SRN
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FDA FEI Number
3011191255
DUNS Number
047025993

Catalogue (1790)

Page 6 of 36
DeviceModel / ReferenceRegistriesClassStatus
Vive LVA3078WHTL
FDA UDI
Class IActive
Vive SUP3078BLKS
FDA UDI
Class IActive
ViveSole INS1051M
FDA UDI
Class IActive
Vive Health LVA2098
FDA UDI
Class IActive
Vive Health SUP1037S
FDA UDI
Class IActive
Vive Mobility MOB1027RED
FDA UDI
Class IIActive
ViveCare LVA3076PMP
FDA UDI
Class IIActive
Vive INS1033WHT
FDA UDI
Class IActive
Sures LVA1058KNG2
FDA UDI
Class IActive
Vive MOB1001PUR
FDA UDI
Class IActive
BioTab RHB3023BLKL
FDA UDI
Class IIActive
CoreTech SUP2031BLK
FDA UDI
Class IActive
Vive SUP1082BLU
FDA UDI
Class IActive
Vive SUP3077BLKUNI
FDA UDI
Class IActive
CoreTech SUP2035BLKL
FDA UDI
Class IActive
Vivesole INS1005S
FDA UDI
Class IActive
Vive LVA3080PAK3
FDA UDI
Class IActive
ViveCare RHB2075TAN48
FDA UDI
Class IActive
Vive SUP1026
FDA UDI
Class IActive
CoreTech SUP2033BLKXS
FDA UDI
Class IActive
Vive RHB1099PAK
FDA UDI
Class IActive
Vive SUP3082BLKL
FDA UDI
Class IIActive
Vive Mobility MOB1010RED
FDA UDI
Class IActive
Vive SUP1041PAK2
FDA UDI
Class IActive
Vive SUP3080BLKL
FDA UDI
Class IIActive
CoreTech SUP2028BLKXS
FDA UDI
Class IActive
Vive MOB1017BLK
FDA UDI
Class IActive
ViveCare RHB3030S10CT
FDA UDI
UActive
ViveSole INS10564XL
FDA UDI
Class IActive
Vive SUP3047BLKS
FDA UDI
Class IActive
Vive SUP3047BLKXL
FDA UDI
Class IActive
Vive LVA1025WLC
FDA UDI
Class IActive
Arctic Flex RHB3009BLKXL
FDA UDI
Class IActive
ViveSole INS1047BLUS
FDA UDI
Class IActive
ViveSole INS1047BLKL
FDA UDI
Class IActive
CoreTech SUP3056BLK
FDA UDI
Class IActive
Vive SUP3008BGE
FDA UDI
Class IActive
Vive LVA2029
FDA UDI
Class IActive
Vive LVA1087OS
FDA UDI
Class IActive
Vive MOB1002BBT
FDA UDI
Class IActive
CoreTech SUP3091BLKTXS
FDA UDI
Class IActive
Vive Mobility MOB1105BLK
FDA UDI
Class IActive
CoreTech SUP3073BLKXS
FDA UDI
Class IActive
Vive SUP2038
FDA UDI
Class IActive
Vive LVA1021
FDA UDI
Class IActive
Vive SUP3020XXL
FDA UDI
Class IActive
Vive SUP3027BLK
FDA UDI
Class IActive
Vive LVA3090BLUS250CT
FDA UDI
Class IActive
Vive LVA3093
FDA UDI
Class IActive
Vive MOB1032
FDA UDI
Class IActive

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