Medical Device Manufacturer · US , Hanover , MA

Denali Corporation - FDA 510(k) Cleared Devices

9 submissions · 9 cleared · Since 2007

Total

Cleared

Denied

Denali Corporation has 9 FDA 510(k) cleared medical devices. Based in Hanover, US.

Historical record: 9 cleared submissions from 2007 to 2016. Primary specialty: Dental.

Browse the FDA 510(k) cleared devices submitted by Denali Corporation Filter by specialty or product code using the sidebar.

Denali Corporation is one of 4827 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Denali Corporation

9 devices

1-9 of 9

AURALAY PIT & FISSURE SEALANT

K071158 · EBC

Dental · 41d

Cleared May 10, 2007

FUSION RESIN CEMENT AND CORE KIT

K070702 · EBF

Dental · 58d

Cleared May 09, 2007

AURAVUE PIT & FISSURE SEALANT

K070693 · EBF

Dental · 57d

Denali Corporation - FDA 510(k) Cleared Devices

FDA 510(k) Regulatory Record - Denali Corporation

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