Danville Materials, Inc.
Danville Materials, Inc. holds FDA 510(k) medical device clearances, first cleared 2001, most recent 2012, with 1 FDA device recall on record.
Top product codes for Danville Materials, Inc.
FDA recalls by Danville Materials, Inc.
Recalls are matched by FDA's recalling-firm name — openFDA's enforcement dataset doesn't reference 510(k) numbers, so a recall here may cover devices beyond this company's 510(k) clearances.
Recent clearances by Danville Materials, Inc.
- K121880 — DMRC NANOFLOW DMRC NANOCOMPOSITE EBOND SURE ETCH GEL SURE ETCH LIQUID
- K111876 — Z BOND, PRELUDE ONE
- K110642 — SILJETR SYSTEM
- K102753 — TURBO TEMP 3
- K092912 — STARFILL 2B HV (HIGH VISCOSITY) ROCKCORE, MODEL: 90838 AND STARFILL 2B LV (LOW VISCOSITY), MODEL: 90150
- K092319 — STAR VPS, MODEL 80014-01, FIRST QUATER, MODEL 90649, FIRST HALF, MODEL 89387
- K090106 — PRELUDE ONE
- K040952 — PRELUDE
- K033215 — PREPAIR
- K020760 — STARFLOW HV
- K012354 — SNOWPOST, SNOWLIGHT
Data sourced from openFDA. This site is unofficial and independent of the FDA.