Medical Device
Manufacturing
THE TRADE PAPER OF THE FACTORY FLOOR
K844662Substantially Equivalent

Kerr Herculite Dental Composite Restorative Materi

Kerr Corporation (Danbury), Washington DC / Traditional, Substantially Equivalent

K844662 is the FDA 510(k) clearance record for KERR HERCULITE DENTAL COMPOSITE RESTORATIVE MATERI, a class II device, cleared for Kerr Corporation (Danbury) on under FDA product code EBF (Material, Tooth Shade, Resin). FDA records list 32 510(k) clearances for Kerr Corporation (Danbury), from to . As of , FDA records show no recalls naming K844662.

Clearance record

Decision date
Received
(115 days to decision)
Product code
EBF Material, Tooth Shade, Resin
Regulation
21 CFR 872.3690
Device class
Class II
Review panel
Dental
Applicant
Kerr Corporation (Danbury) Suite 1200, Washington DC
Third party review
No

Clearances, product code EBF

Trailing 12 months
19 clearances under product code EBF in the twelve months to October 2026, April 2026 the highest month at 5.
Show the numbers
Monthly 510(k) clearances under FDA product code EBF, trailing twelve months
MonthClearances
November 20251
December 20251
January 20261
February 20260
March 20262
April 20265
May 20262
June 20262
July 20262
August 20261
September 20262
October 20260