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Revolution Formula 2

Kerr Corporation · Model 34983 · UDI-DI 00841396110405

EBF Prescription
10
510(k) clearances
961
Adverse events (1 deaths)
0
Recalls
206
Facilities

Description

Flowable Light Cure Composite; Syringe; XL; Refill

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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.