Skip to content

Celleva Inc. · Innovating healing

One company, two platforms, one standard.

Celleva develops regenerative biologics from Goyang-si, South Korea, across two complementary production platforms.

Different scientific objectives, product specifications, markets and regulatory environments call for different levels of biological complexity, molecular definition and process control. Running two platforms is what lets the manufacturing route be chosen against the application.

PEXT development is carried out in collaboration with the scientific team at Seoul National University, and production is operated in compliance with cGMP and cGLP standards.

Celleva Inc.

Not every application requires the same product. Every application requires the same commitment to measurable quality.

Headquarters
Suite #506, 656 Gwonyuldae-ro, Deogyang-gu, Goyang-si, Gyeonggi-do, South Korea 10654
Research collaboration
Seoul National University, South Korea
Manufacturing standards
cGMP · cGLP
Brand
PEXT™ · Premium Exosomes Therapy
Visit cell-eva.com
The PEXT brandmark

PEXT

The name

PEXT stands for Premium Exosomes Therapy.

The mark is the ornament stamped on every vial. On this platform “premium” is not a grade of packaging. It is the claim that the producer cells were measured before anything was made from them, and that the measurements travel with the lot.

Scientific direction

Who stands behind the science

Claims about source-cell selection, characterization and regulatory position are made under a named scientific direction, not an anonymous corporate voice.
Prof. Dr. H. Eray Copcu, MD, Scientific Director at Celleva Inc.

Prof. Dr. H. Eray Copcu, MD

Scientific Director

Plastic, Reconstructive and Aesthetic Surgery · Regenerative Medicine

Professor of Plastic, Reconstructive and Aesthetic Surgery, and the first academic in Turkey to establish a regenerative medicine department at a university.

Prof. Dr. H. Eray Copcu has worked on stromal-cell and regenerative treatment technologies since becoming a professor in 2011, across Turkey and Korea. He founded the aesthetic and plastic surgery departments at the medical faculties of both Adnan Menderes University and Izmir University, and went on to found the first regenerative medicine department in a Turkish university.

His research interests are cell therapy, stem cells and preadipocytes, alongside aesthetic and reconstructive breast surgery. He holds patents in stromal-cell transfer, and developed the MEST, ARAT and Supercharged MEST techniques now used internationally.

Title
Professor of Plastic, Reconstructive and Aesthetic Surgery
Medical degree
Ege University Medical Faculty, Izmir
Residency
Izmir Ataturk Teaching and Research Hospital
Professorship
Adnan Menderes University, 2011
Founded
First regenerative medicine department in a Turkish university
Former roles
Vice Dean, Medical Faculty, Adnan Menderes University; Head of Surgical Disciplines, Izmir University
Current
Founder, MEST Aesthetic Plastic Surgery Center, Izmir; Founder, G-CAT (Gene, Cell and Tissue) Academy, Istanbul
Societies
Member and National Delegate, ISPRES (International Society of Plastic and Regenerative Surgeons)
Editorial
Editor-in-Chief, Internet Journal of Plastic Surgery; editorial boards of several international journals
Publications
More than 70 peer-reviewed articles in international journals
Techniques developed
MEST (Mechanical Stromal-cell Transfer), ARAT (Adjustable Regenerative Adipose-tissue Transfer), Supercharged MEST

Core competencies

What the company is built to do

Source-cell assessment
Glutathione-based selection of producer-cell populations using the FreSHtracer platform, before any production run begins.
Clean EV manufacture
Phenol red-free, animal component-free culture and a controlled multi-step isolation and purification workflow.
Recombinant protein production
Sequence-defined human protein expression in a controlled microbial system, without human producer cells.
Characterization & release
Identity, purity, composition, potency and stability testing organized as a published per-lot record.

Two pathways. One standard.

Pick the platform that fits the work.