510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K852476Substantially Equivalent

Interplak

Dental Research Corp., Tucker GA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K852476 is the FDA 510(k) clearance record for INTERPLAK, a class I device, cleared for Dental Research Corp. on under FDA product code JEQ (Toothbrush, Powered). FDA records list one 510(k) clearance for Dental Research Corp. As of , FDA records show no recalls naming K852476.

Clearance record

Decision date
Received
(50 days to decision)
Product code
JEQ Toothbrush, Powered
Regulation
21 CFR 872.6865
Device class
Class I
Review panel
Dental
Applicant
Dental Research Corp. 1728 Montreal Cir., Suite 27, Tucker GA
Third party review
No

Clearances, product code JEQ

Trailing 12 months

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

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