2nd Choice Silver Wave Compression Leggings, 40-95 kg Weight Class 1

Micro-massaging, opaque, stretchy leggings with graduated compression of 15/21 mmHg.

These leggings have minor imperfections. That’s why you can save significantly. Please note that they cannot be exchanged.

The particularly stretchy hip panel wraps around the hips and fits beautifully on curvier figures, with an excellent fit that accommodates up to two sizes larger.
Extra opaque, perfect for wearing out in public. The special 3D wave fabric delivers a soothing micro-massage that stimulates microcirculation and can eliminate excess water retention.
The breathable, antimicrobial-treated material prevents unpleasant odors from forming. Made from a yarn with a Far Infrared (FIR) mineral additive, it stimulates the body’s natural thermal energy, converts it into infrared rays, and releases it back to the skin tissue with a pleasant heat-regulating effect.
Tightens and enhances the appearance of the thighs, buttocks, and abdomen. Features a gusset and flatlock seams.
This medical device is designed to treat and relieve venous and lymphatic reflux, helping to prevent one or more circulatory disorders (e.g., edema, deep vein thrombosis, varicose veins, lymphedema).
This medical device is also suitable as an aid for treating cellulite (orange peel skin), managing lipedema, and for daily and athletic activities.

These leggings have a higher compression level than the Wonder Leggings.
For anyone who wants a bit more compression

(You will need a little extra effort to put them on—don’t worry, you won’t need rubber gloves for this either).

These leggings fit wearers up to 195cm tall and 150kg in weight.If you need help finding your correct size, please reach out—we would be happy to assist you wholeheartedly.

For first aid use PO

Here’s the secret: the internal, performance-focused wave panels.

And an extra bonus :-) They have a matte finish

Solidea’s "Graduated Compression Medical Products for Limbs and Body" line is classified under Class I, Rule 1 in accordance with the regulations outlined in Annex VIII of the European Medical Device Regulation 2017/745. Technical documentation and post-market surveillance are conducted in accordance with Annexes II and III of the aforementioned European Regulation.