Prollenium Medical

Revanesse® Versa™

hyaluronic acid dermal filler

Revanesse Versa is a hyaluronic acid filler made by Prollenium Medical Technologies, a Canadian company based in Aurora, Ontario. Like other hyaluronic acid fillers, it is a gel made from a sugar molecule already present in skin, injected beneath the surface to smooth lines and folds. The product falls under an FDA approval (PMA P160042) originally granted in August 2017 under the trade name Revanesse Ultra, with the Versa formulation added to that same approval afterward; the approved indication covers injection into the mid-to-deep dermis to correct moderate to severe facial wrinkles and folds, such as nasolabial folds, in adults 22 and older. Prollenium's current site markets the product as Revanesse Versa+, alongside a related lip-specific product, Revanesse Lips+. Prollenium describes its products as researched, designed, and manufactured in-house, without naming a specific branded cross-linking process in its public materials.

The record

  • FDA approved the underlying PMA (P160042) on August 4, 2017, originally under the trade name Revanesse Ultra, for injection into the mid-to-deep dermis to correct moderate to severe facial wrinkles and folds, such as nasolabial folds, in adults 22 and older.
  • Manufacturer is Prollenium Medical Technologies, Inc., based in Aurora, Ontario, Canada.
  • The current product line on Prollenium's own site is marketed as Revanesse Versa+ and Revanesse Lips+.

Where this came from

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Revanesse® Versa™ and its logo belong to Prollenium Medical Technologies, Inc. (Aurora, Ontario, Canada). This page describes equipment and products used at UDERMA Medspa & Laser; it is general information, not medical advice, and whether this one suits you is a conversation to have at a consultation.

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