510(K) CLEARANCES 67 ▼8RECALLS POSTED 26CLASS I 2PMA DECISIONS 40 ▼14WEEK ENDING / FDA DATA AS OF
Medical Device
ManufacturingTHE TRADE PAPER OF THE FACTORY FLOOR
SUBSCRIBE / SIGN IN
K923980Substantially Equivalent

Q3 Disposable Prophy Angle

Q3 Special Products, Inc., St. Louis MO / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K923980 is the FDA 510(k) clearance record for Q3 DISPOSABLE PROPHY ANGLE, a class I device, cleared for Q3 Special Products, Inc. on under FDA product code EGS (Handpiece, Contra- And Right-Angle Attachment, Dental). FDA records list one 510(k) clearance for Q3 Special Products, Inc. As of , FDA records show no recalls naming K923980.

Clearance record

Decision date
Received
(293 days to decision)
Product code
EGS Handpiece, Contra- And Right-Angle Attachment, Dental
Regulation
21 CFR 872.4200
Device class
Class I
Review panel
Dental
Applicant
Q3 Special Products, Inc. 511 Sarah Ln., St. Louis MO
510(k) summary
Statement
Third party review
No

Clearances, product code EGS

Trailing 12 months

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

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