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VAIM Co., Ltd.

South Korea·KR-MF-000026357

Last updated September 18, 2026

About

Juvelook Volume (Juvelook Volume), Juvelook Manufacturing Company, Leaders who pioneer new trends in the field of tissue regeneration products and improvement medical devices such as fillers

Translated from the manufacturer's own website. Source

What VAIM Co., Ltd. makes

VAIM Co., Ltd. manufactures injectable dermal fillers, including Juvelook Glam, Juvelook Volume, and Juvelook, which are designed for soft tissue augmentation and volume restoration. The company also produces Lenisna, a device for skin tightening and contouring, and Vivabella, intended for aesthetic enhancement procedures. These products are primarily used in cosmetic and reconstructive treatments to improve facial and body contours.

The company’s portfolio is classified under Class III medical devices, indicating high-risk products requiring stringent regulatory oversight. These devices are registered in the EU’s eudamed database, ensuring compliance with European Union medical device regulations. VAIM Co., Ltd. is based in South Korea.

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 VAIM Co., Ltd. manufacture?

VAIM Co., Ltd. specializes in injectable dermal fillers and skin contouring devices. Their portfolio includes products like Juvelook Glam, Juvelook Volume, and Juvelook, which are designed for soft tissue augmentation and volume restoration. Additionally, they produce Lenisna for skin tightening and Vivabella for aesthetic enhancement, primarily used in cosmetic and reconstructive treatments.

Where is VAIM Co., Ltd. based?

VAIM Co., Ltd. is headquartered in South Korea. The company’s location influences its regulatory compliance framework, particularly for devices marketed in regions like the European Union.

Which regulatory registries list VAIM Co., Ltd.’s devices?

VAIM Co., Ltd.’s devices are registered in the EU’s eudamed database, which is the official portal for medical device information under European Union regulations. This ensures transparency and compliance with EU requirements for high-risk medical devices.

How are VAIM Co., Ltd.’s devices classified under medical device regulations?

VAIM Co., Ltd.’s devices fall under Class III classification, which is the highest risk category for medical devices. This classification applies to products like injectable fillers and skin contouring devices due to their potential risks, such as infection, adverse reactions, or permanent damage, requiring rigorous pre-market authorization and post-market surveillance.

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

Information

Country
South Korea
Address
14, Techno 3-ro, Yuseong-gu, Daejeon, South Korea
LinkedIn
—
Facebook
—
Phone
+82 42 935 6456
PRRC Contact
Dongseob Kwak
EUDAMED SRN
KR-MF-000026357
FDA FEI Number
—
DUNS Number
—

Catalogue (6)

DeviceModel / ReferenceRegistriesClassStatus
Juvelook Glam VA2001
EUDAMED
Class IIIActive
Juvelook Volume VA1054
EUDAMED
Class IIIActive
Lenisna VA1052
EUDAMED
Class IIIActive
Vivabella VA1081
EUDAMED
Class IIIActive
Juvelook VA1002
EUDAMED
Class IIIActive
Lenisna VA1011
EUDAMED
Class IIIActive

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