510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K791133Substantially Equivalent

Abcor Caries Detector Monitor

Abcor, Inc., Mchenry IL / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K791133 is the FDA 510(k) clearance record for ABCOR CARIES DETECTOR MONITOR, a class II device, cleared for Abcor, Inc. on under FDA product code LFC (Device, Caries Detection). FDA records list one 510(k) clearance for Abcor, Inc. As of , FDA records show no recalls naming K791133.

Clearance record

Decision date
Received
(71 days to decision)
Product code
LFC Device, Caries Detection
Regulation
21 CFR 872.1740
Device class
Class II
Review panel
Dental
Applicant
Abcor, Inc. 803 N. Front St. Suite 3, Mchenry IL
Third party review
No

Clearances, product code LFC

Trailing 12 months

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

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