Drug intelligence / Profile preview

Biovance 3L Ocular

Development stage
Unknown
Lead developer
Celularity
Administration
Ophthalmic
01

Overview

Biovance 3L Ocular is a three-layer decellularized, dehydrated, human amniotic membrane biologic medical device. Developed by Celularity and distributed exclusively in the United States by Verséa Ophthalmics, it is designed as a biological membrane covering that provides an extracellular matrix (ECM) to support the healing of advanced ocular surface diseases. The allograft consists of three layers of amniotic membrane that act as a barrier to protect underlying tissue and preserve tissue plane boundaries. It is indicated for various ocular conditions, including corneal epithelial defects, pterygium repair, and fornix reconstruction, and can be applied either surgically or topically to the ocular surface. The product is regulated by the FDA as a human tissue-based product under Section 361 of the Public Health Service Act.

Brand names
Biovance 3L OcularBiovance3L OcularBiovance-3L OcularBiovance
Other names
Biovance 3LBiovance3LBiovance-3L

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