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Mysmile

ABrite Tech (Shanghai) Co., Ltd. · Model LP211-BK-MS · UDI-DI 06977957550008

EFS

510(k) clearances

215

Adverse events

Recalls

220

Facilities

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Data compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.