| PCL* | GOURI, Ellanse | Fully liquid / Particle suspension | No particles / Microspheres | Approx.24–36 months | Fibroblast activation, type I/III collagen synthesis | Longest biodegradation period |
| PLLA* | Sculptra | Powder → Suspension | Irregular microspheres (40–63 ㎛) | Approx.18–24 months | Fibroblast stimulation via macrophage phagocytosis | Longest clinical data, FDA* approval;MFDS* approved lidocaine co-use (2023) |
| PDLLA* | Juvelook, AestheFill | Powder → Suspension (HA* or CMC* carrier) | Spherical porous microspheres (30–70 ㎛) | Approx.9-12 months (faster than PLLA) | Same mechanism as PLLA; faster degradation due to amorphous structure | Simultaneous HA effect expected |
| PDO* | ULTRACOL | Powder → Suspension (SCMC carrier) | Fine particles (lyophilized powder) | Approx.4–9 months | Fibroblast stimulation and collagen synthesis during biodegradation | Shortest biodegradation period; mainly used as solid thread; liquid-type rare |
| CaHA* | RADIESSE, VOLassom | Suspension (gel carrier) | Spherical microspheres (25–45 ㎛) | Approx.12–18 months | Immediate volumizing effect of CaHA microspheres;fibroblast stimulation via Ca²⁺/PO4³⁻ ion release upon degradation (dual mechanism) | RADIESSE+ Lidocaine (0.3% pre-mixed) import-approved domestically (2017) |