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Warwick James Root Elevator

SONTEC INSTRUMENTS, INC. · Model 1102-WJ-S · UDI-DI 00192896105348

EMJ Prescription

510(k) clearances

641

Adverse events

Recalls

241

Facilities

Description

Warwick James Root Elevator Straight

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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.