Company Brief Introduction
FITAKH was established in 2020, headquatered in Huadu district, Guangzhou
City. We're professional manufacturer focusing on R&D and
production of biodegradable and high-end regenerative microspheres
(including PLLA, PDLLA,CaHA, PCL) and cosmetic peptide raw
materials.
Holds valid Class II Medical Device Production License issued by
China NMPA, passes ISO13485 international quality system
certification and GMP compliance audit. Supported by our in-house
professoinal R&D laboratory and senior registration compliance
expert team. FITAH has always adhered to innovative research on
raw‑material technologies, continuously developing high‑quality and
compliant regenerative biomaterials. Going forward, we will join
hands with global partners to explore the vast market of
regenerative medical aesthetic, and drive the standardized and
high‑quality development of the aesthetic‑medical raw‑material
industry.
Core Advantages·Why Choose Us
♦ Solid Qualifications
Master File(MDMF) Registration completed for
full‑range raw materials(PCL / PLLA / CaHA / PDRN / Silk fibroin /
Recombinant collagen)
♦ University‑Enterprise Collaborative Technical Team
UCTC(University of Science and Technology of China)
Biomedical PhD Team
♦ Full‑range Testing with Traceable Data
·Particle size detection(SEM+laser)
·Biocompatibility test report
·Degradation cycle test(Q/FTF1688S-2025)
·Sterility testingµbial limit(CHP/USP dual standard)
♦ Reliable Delivery Capacity
·Factory direct supply
·Dual system of R&D & mass production
·Degradation cycle test(Q/FTF1688S-2025)
·Strict internal quality control, consistent batch
performance, identical quality between samples and contract goods
