Our key milestones

Our key milestones

  • 2018
    • RHA® topical skin booster (depending on country registration)

      1st* professional sterile crosslinked High Molecular Weight - Hyaluronic Acid based topical product including active ingredients maintaining aesthetic procedure results.

  • 2018
    • Opening of the TEOXANE Academy in Geneva

      Ability to welcome doctors into the heart of TEOXANE headquarters in Switzerland.

  • 2017
    • FDA approval RHA® 2 | RHA® 3 | RHA® 44

      Opening of a second production line. FDA approval for RHA®2, RHA®3, RHA®4 for the correction of moderate to severe dynamic facial wrinkles and folds.

  • 2015
    • TEOSYAL RHA® line (depending on country registration)

      Launch of the Resilient Hyaluronic Acid gel line: TEOSYAL®RHA for Dynamic Aesthetics. A novel cross-linking technology that adapts to the movements and dynamism of the face.

  • 2014
    • TEOSYAL® PEN(depending on country registration)

      The 1st* motorised, cordless hyaluronic acid injection system - more precise injections for practitioners coupled with reduced pain for patients.

  • 2012
    • TEOSYAL® PURESENSE REDENSITY1 line (depending on country registration)

      2 groundbreaking launches that changed anti-ageing approaches:  a dermal filler, Redensity 2 , specifically designed as an under-eye circle fighter and a cocktail of free HA and nutriments, Redensity  1, renown worldwide as a unique beauty booster

  • 2011
    • TEOSYAL®PURESENSE1 range, with Lidocaine (depending on country registration)

      TEOXANE is the 3rd manufacturer to master the addition of lidocaine in dermal fillers, creating the TEOSYAL® PURESENSE range, for a more comfortable injection experience

  • 2009
    • TEOXANE Cosmeceuticals(depending on country registration)

      Creation of TEOSYAL® Cosmeceuticals range – A perfect complement to facial aesthetic procedures

  • 2006
    • TEOSYAL® ULTRA DEEP & KISS® (depending on country registration)

      TEOSYAL® ULTRA DEEP1 , 1st* volumizer developed to be injected using a needle. TEOSYAL KISS®1 the 1st* specific filler dedicated to lip treatment.

  • 2004
    • TEOSYAL® Classic1 range (depending on country registration)

      A state-of-the art range of hyaluronic acid-based dermal fillers that allows practitioners  to address the main rejuvenation concerns.

  • 2003
    • TEOXANE establishment in Geneva, Switzerland

      Creation of TEOXANE Laboratories in Geneva, Switzerland.

References

*at Teoxane Laboratories

  1. All products of the TEOSYAL® Classic, TEOSYAL® PURESENSE and TEOSYAL RHA® lines, including TEOSYAL® ULTRA DEEP, TEOSYAL KISS®, TEOSYAL PURESENSE ® REDENSITY 1 & 2, and TEOSYAL RHA® 1 to 4, are trademarks of the firm TEOXANE SA. They are class III medical devices and are regulated health products bearing the CE marking (CE0086) under this regulation. They are available in around 80 countries, excluding the US. For professional use only. Please refer to instructions for use. TEOSYAL® PURESENSE and TEOSYAL® RHA products are gels that contain hyaluronic acid, and 0.3% by weight of lidocaine hydrochloride (local anaesthetic can induce a positive reaction to anti-doping tests).
  2. Products of the TEOXANE Cosmeceutical range are cosmetic products according to European Regulation 1223/2009, except Radiant Night Peel which is a class I medical device, according to Directive 93/42/EEC. Cosmeceuticals products are not designed to be injected.
  3. TEOSYAL® PEN is a non-sterile class IIa medical device (CE0434) intended to assist medical practitioner for dermal filler injections. Manufactured by JuvaPlus in Switzerland. For more information, please consult the user guide of TEOSYAL® PEN or the recommendations available on www.teosyalpen.com. Please refer to instructions for use. It is the practitioner’s full responsibility to read and inform the patient about adverse reaction.
  4. RHA® is a trademark of TEOXANE SA. RHA® 2, RHA® 3, RHA® 4 are products of TEOXANE SA. They are class III medical devices and have received FDA approval but are not yet commercialized in the United States. The United States Federal law restricts these devices to sale by or on the order of a physician or license practitioner. RHA® 2, RHA® 3 and RHA® 4 are indicated for the correction of moderate to severe dynamic facial wrinkles and folds, such as nasolabial folds (NLF), in adults aged 22 years or older. RHA® 2, RHA® 3, and RHA® 4 are sterile gels containing crosslinked hyaluronic acid in physiological buffer and 0.3% lidocaine hydrochloride to reduce pain on injection. RHA® 2, RHA® 3 and RHA® 4 are contraindicated in patients with previous hypersensitivity to local anaesthetics of the amide type, such as lidocaine. Please refer to the Instructions for Use (https://www.accessdata.fda.gov/cdrh_docs/pdf17/P170002C.pdf). It is the practitioner’s full responsibility to read and inform the patient about contraindications, warnings, precautions, risks and benefits.

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