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Symphion

BOSTON SCIENTIFIC CORPORATION · Model FG-0201 · UDI-DI 08714729863656

PGT Prescription
3
510(k) clearances
122
Adverse events (2 deaths)
0
Recalls
5
Facilities

Description

Tissue Removal System Resecting Device

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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.