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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
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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 2 of 36
DeviceModel / ReferenceRegistriesClassStatus
ViveCare RHB2083M
FDA UDI
Class IActive
Vive SUP3013BLK3XL4P
FDA UDI
Class IActive
CoreTech SUP2032BLKM
FDA UDI
Class IActive
Vive SUP1045
FDA UDI
Class IActive
Vive LVA3046PAK4
FDA UDI
Class IActive
Vive INS1041TLS
FDA UDI
Class IActive
Vive INS1011
FDA UDI
Class IActive
Vive SUP3022BLKGRYS
FDA UDI
Class IActive
TruCompress SUP1086BPS
FDA UDI
Class IActive
Arctic Flex RHB2090TAL
FDA UDI
Class IActive
Vive SUP1059BGE
FDA UDI
Class IActive
Vive MOB1003BLU
FDA UDI
Class IActive
Vive LVA3069S
FDA UDI
Class IIActive
CoreTech SUP3091BLKSS
FDA UDI
Class IActive
CoreTech SUP3072BLKR
FDA UDI
Class IActive
Vive LVA1073STL
FDA UDI
Class IActive
Vive LVA3031BAG
FDA UDI
Class IActive
CoreTech SUP3037BLKXL
FDA UDI
Class IActive
Vive INS1004L
FDA UDI
Class IActive
Vive CSH1049L
FDA UDI
Class IActive
Vive MOB1025SLV
FDA UDI
Class IIActive
Vive MOB1002PUR
FDA UDI
Class IActive
Vive RHB1043WHT
FDA UDI
Class IIActive
Vive SUP1059
FDA UDI
Class IActive
Vive SUP3081BGEL
FDA UDI
Class IIActive
Vive RHB2096BLKS
FDA UDI
Class IActive
Vive SUP1052PAK2
FDA UDI
Class IActive
Vive SUP1089GRY
FDA UDI
Class IActive
BioTab RHB3044S2PAK
FDA UDI
Class IIActive
ViveCare RHB3056WHT44CT5
FDA UDI
UActive
ViveSole INS1057DBLUXS
FDA UDI
Class IActive
Vive SUP2020
FDA UDI
Class IActive
Vive RHB3010BLU
FDA UDI
Class IActive
ViveCare RHB2974XL
FDA UDI
Class IActive
ViveCare RHB2081S
FDA UDI
Class IActive
Vive RHB2029BLK
FDA UDI
Class IIActive
CoreTech SUP2062BLKS
FDA UDI
Class IActive
CoreTech SUP3059BLKXL
FDA UDI
Class IActive
ViveCare LVA3075FLG24
FDA UDI
Class IIActive
Vive MOB1003BRZ
FDA UDI
Class IActive
Vive Mobility MOB1010BLK
FDA UDI
Class IActive
Vive SUP1021L
FDA UDI
Class IActive
Arctic Flex SUP2017RPAK
FDA UDI
Class IActive
ViveSole INS1056BLKXL
FDA UDI
Class IActive
Vive LVA1060GRYL
FDA UDI
Class IIActive
BioTab RHB3023BLKMW
FDA UDI
Class IIActive
Vive DMD1017BLK
FDA UDI
Class IActive
Vive SUP3041BGEXL
FDA UDI
Class IActive
Vive RHB1099S
FDA UDI
Class IActive
Vive MOB1002BFL
FDA UDI
Class IActive

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