510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
Medical Device
ManufacturingTHE TRADE PAPER OF THE FACTORY FLOOR
SUBSCRIBE / SIGN IN
K080089Substantially Equivalent

Sonicflex 2003 and Sonicflex Lux 2003 L with Instrument Tips

Sybron Dental Specialties, Inc., Orange CA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K080089 is the FDA 510(k) clearance record for SONICFLEX 2003 AND SONICFLEX LUX 2003 L WITH INSTRUMENT TIPS, a class II device, cleared for Sybron Dental Specialties, Inc. on under FDA product code ELC (Scaler, Ultrasonic). FDA records list 176 510(k) clearances for Sybron Dental Specialties, Inc., from to . As of , FDA records show no recalls naming K080089.

Clearance record

Decision date
Received
(234 days to decision)
Product code
ELC Scaler, Ultrasonic
Regulation
21 CFR 872.4850
Device class
Class II
Review panel
Dental
Applicant
Sybron Dental Specialties, Inc. 1717 W. Collins Ave., Orange CA
510(k) summary
Summary PDF
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