Medical Device
Manufacturing
THE TRADE PAPER OF THE FACTORY FLOOR
K922380Substantially Equivalent

Bite Rim Wax

Dentsply Intl., York PA / Traditional, Substantially Equivalent

K922380 is the FDA 510(k) clearance record for BITE RIM WAX, a class I device, cleared for Dentsply Intl. on under FDA product code EGD (Wax, Dental, Intraoral). FDA records list 291 510(k) clearances for Dentsply Intl., from to . As of , FDA records show no recalls naming K922380.

Clearance record

Decision date
Received
(27 days to decision)
Product code
EGD Wax, Dental, Intraoral
Regulation
21 CFR 872.6890
Device class
Class I
Review panel
Dental
Applicant
Dentsply Intl. 570 W. College Ave., York PA
510(k) summary
Summary
Third party review
No

Clearances, product code EGD

Trailing 12 months

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

FDA records show no clearances under product code EGD in the twelve months to October 2026.
Show the numbers
Monthly 510(k) clearances under FDA product code EGD, 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