Medical Device
Manufacturing
THE TRADE PAPER OF THE FACTORY FLOOR
K913152Substantially Equivalent

Whiter Biter Crown

George M. Wilson, Dds, Porterville CA / Traditional, Substantially Equivalent

K913152 is the FDA 510(k) clearance record for WHITER BITER CROWN, a class I device, cleared for George M. Wilson, Dds on under FDA product code ELZ (Crown, Preformed). FDA records list 3 510(k) clearances for George M. Wilson, Dds, from to . As of , FDA records show no recalls naming K913152.

Clearance record

Decision date
Received
(75 days to decision)
Product code
ELZ Crown, Preformed
Regulation
21 CFR 872.3330
Device class
Class I
Review panel
Dental
Applicant
George M. Wilson, Dds 380 W. Putnam, Porterville CA
510(k) summary
Statement
Third party review
No

Clearances, product code ELZ

Trailing 12 months

FDA records hold no clearances under product code ELZ in the trailing twelve months.

FDA records show no clearances under product code ELZ in the twelve months to October 2026.
Show the numbers
Monthly 510(k) clearances under FDA product code ELZ, trailing twelve months
MonthClearances
November 20250
December 20250
January 20260
February 20260
March 20260
April 20260
May 20260
June 20260
July 20260
August 20260
September 20260
October 20260