Delta-Lite Casting Resin

No FDA recalls on record, checked 22 Oct 2026.

510(k) Number

K854554 ↗

FDA Product Code

LGF

Device Class

Class I

Regulation

21 CFR Part 888.5940

Advisory Committee

Orthopedic

FDA Decision

SESE Substantially Equivalent

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See all devices from Johnson & Johnson Professionals, Inc. →