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ReMedium

ReMedium Advance H

Hard cross-linked hyaluronic-acid body filler (20 mg/ml, 10 ml) for upper-buttock fullness and projection.

Variants

Volume
10 ml

Specifications

Brand

Manufacturer
Forever18 International Co., Ltd.
Country Of Origin
South Korea

Composition

HA concentration
20 mg/ml
Cross-linking technology
Monophasic
Contains lidocaine
Not Contains
Cross-linking agent
DVS

Treatment

Treatment areas
Body contouring, Buttocks
Longevity
12 months

Regulatory

Country of origin
South Korea
Regulatory status
  • CE mark

Packaging

Storage temperature
Room temperature (up to 25 °C)

Overview

ReMedium Advance H is the hard formulation of the ReMedium Advance range, a cross-linked hyaluronic-acid (HA) body filler made of HA microbeads. It is positioned by the manufacturer for increasing upper-buttock fullness and projection, improving figure balance and body contouring.

Specifications

  • Formulation: hard
  • Material: cross-linked hyaluronic-acid microbeads
  • HA concentration: 20 mg/ml
  • Presentation: 10 ml
  • Manufacturer: BioPlus Co., Ltd., South Korea

Technology

The ReMedium Advance range uses high-cross-linking HA microbeads and the manufacturer's patented multi-stage cross-linking technology, described as giving high viscosity, cohesiveness, moldability and shape retention.

Compared with Advance S

Advance H is the harder option, positioned mainly for upper-buttock contouring. ReMedium Advance S is the softer option, positioned mainly for breast and upper-body contouring. Both are 20 mg/ml, 10 ml cross-linked HA body fillers.

Safety and use

This is an injectable medical aesthetic product for use by licensed practitioners only. The manufacturer's materials list possible complications including pain, swelling, bruising, itching, infection, allergic reactions, palpable masses, asymmetry, ischemia and skin necrosis. Clinician assessment and post-treatment precautions are recommended. Specifications on this page do not replace the current instructions for use (IFU). Confirm certification, market authorization, composition, particle size and recommended needle or cannula with the manufacturer or an authorized distributor for your country before any clinical decision.

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