510(K) CLEARANCES 75 ▼9RECALLS POSTED 26 ▼13CLASS I 2 ▼4PMA DECISIONS 54 ▲7WEEK ENDING / FDA DATA AS OF
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K943403Substantially Equivalent

Condor Ultrasonic Inserts

Condor Products, Inc., Yorba Linda CA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K943403 is the FDA 510(k) clearance record for CONDOR ULTRASONIC INSERTS, a class II device, cleared for Condor Products, Inc. on under FDA product code ELC (Scaler, Ultrasonic). FDA records list one 510(k) clearance for Condor Products, Inc. As of , FDA records show no recalls naming K943403.

Clearance record

Decision date
Received
(600 days to decision)
Product code
ELC Scaler, Ultrasonic
Regulation
21 CFR 872.4850
Device class
Class II
Review panel
Dental
Applicant
Condor Products, Inc. 4860 Via Piedra, Yorba Linda CA
510(k) summary
Statement
Third party review
No

Clearances, product code ELC

Trailing 12 months
2 clearances under product code ELC in the twelve months to October 2026, January 2026 the highest month at 1.
Show the numbers
Monthly 510(k) clearances under FDA product code ELC, trailing twelve months
MonthClearances
November 20250
December 20250
January 20261
February 20260
March 20261
April 20260
May 20260
June 20260
July 20260
August 20260
September 20260
October 20260