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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
—
Facebook
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Email
—
Phone
—
PRRC Contact
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EUDAMED SRN
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FDA FEI Number
3011191255
DUNS Number
047025993

Catalogue (1790)

Page 4 of 36
DeviceModel / ReferenceRegistriesClassStatus
CoreTech SUP3004BLKM
FDA UDI
Class IActive
Vive Health DMD1063BLK
FDA UDI
Class IIActive
Vive Mobility MOB1087BLU
FDA UDI
Class IActive
Vive LVA1059
FDA UDI
Class IActive
CoreTech SUP2045BLKLXL
FDA UDI
Class IActive
ViveSole INS1046L
FDA UDI
Class IActive
Vive SUP1061
FDA UDI
Class IActive
Vive SUP3089BGEM
FDA UDI
Class IActive
Vive SUP1029PAK2
FDA UDI
Class IActive
Vive MOB1005
FDA UDI
Class IActive
Vive RHB1049RPA
FDA UDI
Class IIUnknown
Vive LVA3060M
FDA UDI
Class IIActive
Vive RHB2087BLK2W105L
FDA UDI
Class IActive
Vive MOB1076WHTSLG
FDA UDI
Class IIActive
Vive RHB3019BLK
FDA UDI
Class IActive
ViveSole INS1048BLKS
FDA UDI
Class IActive
Vive SUP2016BLKS
FDA UDI
Class IIActive
Vive LVA1006GML
FDA UDI
Class IActive
Vive DMD1026GRY
FDA UDI
Class IIActive
ViveSole INS1028DBL
FDA UDI
Class IActive
Vive SUP3047BLKM
FDA UDI
Class IActive
Vive Mobility MOB1133BLK
FDA UDI
Class IActive
ViveCare RHB2075TAN22
FDA UDI
Class IActive
CoreTech SUP2028BLKXL
FDA UDI
Class IActive
CoreTech SUP2027BLKR
FDA UDI
Class IActive
CoreTech SUP3091BLKTXL
FDA UDI
Class IActive
Vive RHB2025
FDA UDI
Class IIActive
Vive SUP3096BLKM
FDA UDI
Class IActive
CoreTech SUP3019BLK9
FDA UDI
Class IActive
Vive SUP3095BLK3XL
FDA UDI
Class IActive
Vive Mobility MOB1079BLU
FDA UDI
Class IActive
Vive LVA3009BLK
FDA UDI
Class IActive
Vive Precision DMD1066WHT
FDA UDI
Class IIActive
Vive Breathe LVA3077MSKDA
FDA UDI
Class IIActive
CoreTech SUP20239BLKXS
FDA UDI
Class IActive
CoreTech SUP3092BLKSS
FDA UDI
Class IActive
Vive Mobility MOB1033BLU
FDA UDI
Class IActive
Vive SUP2098R
FDA UDI
Class IActive
Vive LVA3049BLKCM9
FDA UDI
Class IActive
Vive LVA2104PAK48
FDA UDI
Class IActive
Vive SUP2097L
FDA UDI
Class IActive
Vive RHB1053
FDA UDI
Class IActive
Vive MOB1072TAL
FDA UDI
Class IActive
Vive LVA3085PEN
FDA UDI
Class IIActive
Vive MOB1019BLK
FDA UDI
Class IActive
Vive Mobility MOB1018RED
FDA UDI
Class IActive
Vive SUP1077S
FDA UDI
Class IActive
Vive RHB2096BLKL
FDA UDI
Class IActive
BioTab RHB3044BLKL
FDA UDI
Class IIActive
Sures LVA1058QUE
FDA UDI
Class IActive

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