510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K896565Substantially Equivalent

Dmv(r) Veneer Suction Gripper

DMV Corporation, Zanesville OH / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K896565 is the FDA 510(k) clearance record for DMV(R) VENEER SUCTION GRIPPER, a class I device, cleared for Dmv Corp. on under FDA product code EKJ (Burnisher, Operative). FDA records list one 510(k) clearance for Dmv Corp. As of , FDA records show no recalls naming K896565.

Clearance record

Decision date
Received
(77 days to decision)
Product code
EKJ Burnisher, Operative
Regulation
21 CFR 872.4565
Device class
Class I
Review panel
Dental
Applicant
Dmv Corp. P.O. Box 878, Zanesville OH
Third party review
No

Clearances, product code EKJ

Trailing 12 months

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

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