510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K930151Substantially Equivalent

Omni-Matrix

Innovative Technology, Ltd., Ontario L3y 1j8, CA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K930151 is the FDA 510(k) clearance record for OMNI-MATRIX, a class I device, cleared for Innovative Technology , Ltd. on under FDA product code JEP (Retainer, Matrix). FDA records list 2 510(k) clearances for Innovative Technology , Ltd., from to . As of , FDA records show no recalls naming K930151.

Clearance record

Decision date
Received
(254 days to decision)
Product code
JEP Retainer, Matrix
Regulation
21 CFR 872.4565
Device class
Class I
Review panel
Dental
Applicant
Innovative Technology , Ltd. 227 Eagle St., Ontario L3y 1j8, CA
510(k) summary
Summary
Third party review
No

Clearances, product code JEP

Trailing 12 months

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

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