Plan from the root with RCMS 3.0, draw on 200+ treatment‑plan designers and the M1–M20 module library, manufacture in‑house, and monitor every stage with ART². Not just a tray in a box.
RCMS 3.0 integrates CBCT root/bone data with crown scans — nerve‑canal boundaries, cortical‑bone limits and per‑tooth CR points on every plan.
Color‑coded movement and expression‑rate tracking at every review — catch drift while it is still cheap to correct.
Fully automated 10‑step production at the Shaoxing smart factory — consistent quality and short lead times.
Treatment plan designers holding dental degrees, backed by a PhD and Professor think tank — your plan is never a black box.
Align Digital Case Platform, AI aligning preview, AI cephalometric engine, RCMS 3.0 and the re‑treatment simulation module with achievement‑rate table.
Proven M1–M7 core solutions plus traction, expansion, bite management and skeletal guidance devices — configure what the case needs.
Upload STL scans, photos and X‑rays to the Align Digital Case Platform — STL import in 3 minutes, virtual alignment in 3 seconds.
→RCMS 3.0 + OFS/VBFS compute the plan; your assigned designer refines it; you compare options chairside with the AI aligning preview.
→The approved plan drives the automated line — MagicMove film thermoforming, robotic laser trimming, quality check, sealed shipment.
→ART² superimposition review at every stage; refinements within the tier window keep the case on the achievement‑rate curve.
| P10 | P20 | P40 | Pro | |
|---|---|---|---|---|
| Stages · aligners | 0–10 · ≤20 | 0–20 · ≤40 | 0–40 · ≤80 | Unlimited |
| Refinements | 1× | 2× | 3× | Unlimited |
| Expiration | 1 yr | 3 yrs | 3 yrs | 5 yrs |
| Indication depth | Minimal | Gentle | Medium | Advanced |
YIMEIQI clear aligners are custom-made medical devices under Regulation (EU) 2017/745 (MDR). In accordance with MDR Article 52(8), custom-made devices do not require a Notified Body CE certificate. Compliance is evidenced by the Dutch CIBG registration NL-CA002-2025-83681 and the manufacturer’s Declaration of Conformity (MDR DoC). Manufacturer EUDAMED SRN: CN-MF-000049161.
Guided setup for scanning, case submission and the planning portal — first submission within days, not weeks.
Root‑crown planning workshops, module selection (M1–M20) and case reviews with our medical team.
A dedicated channel for plan questions, mid‑treatment adjustments and refinement requests.
Send us a note and we'll set up a clinical introduction — including tier guidance for your case mix.