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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 7 of 36
DeviceModel / ReferenceRegistriesClassStatus
Vive SUP1016L
FDA UDI
Class IActive
Vive LVA1077PK48
FDA UDI
Class IActive
CoreTech SUP2044BLKRM
FDA UDI
Class IActive
Vive SUP1073S
FDA UDI
Class IActive
Vive SUP1040G
FDA UDI
Class IActive
Vive SUP1046
FDA UDI
Class IActive
Vive SUP1032BGE
FDA UDI
Class IActive
Vivesole INS1010L
FDA UDI
Class IActive
Vive SUP1070PAK2
FDA UDI
Class IActive
Vive LVA2021
FDA UDI
Class IActive
Vive RHB2011BLKS
FDA UDI
Class IActive
Vive Mobility MOB1058BKL
FDA UDI
Class IIActive
Vive LVA2088
FDA UDI
Class IActive
Vive LVA1004
FDA UDI
Class IIActive
Vive SUP1063S
FDA UDI
Class IActive
Vive Health DMD1013BLK
FDA UDI
Class IIActive
Sures LVA1016MBLU
FDA UDI
Class IActive
Vive SUP1037BLKXL
FDA UDI
Class IActive
CoreTech SUP2035BLKXL
FDA UDI
Class IActive
CoreTech SUP2029BLKL
FDA UDI
Class IActive
Vive SUP3044BLK30
FDA UDI
Class IActive
Vive SUP3020XXXXL
FDA UDI
Class IActive
Vive SUP3087BGEM
FDA UDI
Class IActive
CoreTech SUP2025BLK
FDA UDI
Class IActive
CoreTech SUP3091BLKSXS
FDA UDI
Class IActive
Vive MOB1031BLK4
FDA UDI
Class IActive
Vive SUP2019
FDA UDI
Class IActive
Vive SUP1013S
FDA UDI
Class IActive
Vive LVA3078WHTS
FDA UDI
Class IActive
Sures LVA1016M
FDA UDI
Class IActive
Sures LVA3088SUPS
FDA UDI
Class IActive
Vive SUP3095BLK4XL
FDA UDI
Class IActive
CoreTech RHB2086SLEM
FDA UDI
Class IIActive
Vive SUP1019XS2PAK
FDA UDI
Class IActive
Vive SUP3013BLK3XL3P
FDA UDI
Class IActive
Vivesole INS1029WHT
FDA UDI
Class IActive
Vive MOB1011WHT
FDA UDI
Class IActive
Vive DMD1047
FDA UDI
Class IIActive
Arctic Flex RHB2103BLKL
FDA UDI
Class IActive
Vive SUP3047BGE2XL
FDA UDI
Class IActive
Vive Mobility MOB1088MGR
FDA UDI
Class IActive
Vive LVA2053PAK2
FDA UDI
Class IActive
CoreTech SUP2028BLKS
FDA UDI
Class IActive
TruCompress SUP1086BLKM
FDA UDI
Class IActive
CoreTech SUP2079BLKLS
FDA UDI
Class IActive
Vive MOB1041BRZ
FDA UDI
Class IActive
Vive RHB2011BLKM
FDA UDI
Class IActive
Vive LVA1016M4
FDA UDI
Class IActive
Vive LVA1006LPD
FDA UDI
Class IActive
Vive LVA2033
FDA UDI
Class IActive

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