Medical Device
Manufacturing
THE TRADE PAPER OF THE FACTORY FLOOR
K233122Substantially Equivalent

High Speed Air Turbine Handpiece (G100,G200,G300,G400,G450,G500,G600,G700,G700L,G800,G800L)

Litu Tech Ltd., Guangdong, CN / Traditional, Substantially Equivalent

K233122 is the FDA 510(k) clearance record for High Speed Air Turbine Handpiece (G100,G200,G300,G400,G450,G500,G600,G700,G700L,G800,G800L), a class I device, cleared for Litu Tech , Ltd. on under FDA product code EFB (Handpiece, Air-Powered, Dental). FDA records list one 510(k) clearance for Litu Tech , Ltd. As of , FDA records show no recalls naming K233122.

Clearance record

Decision date
Received
(216 days to decision)
Product code
EFB Handpiece, Air-Powered, Dental
Regulation
21 CFR 872.4200
Device class
Class I
Review panel
Dental
Applicant
Litu Tech , Ltd. C1-2 # 12 Denengxi Rd. Torch Zone, Zhongshan, Guangdong, CN
510(k) summary
Summary PDF
Third party review
No

Clearances, product code EFB

Trailing 12 months
3 clearances under product code EFB in the twelve months to October 2026, January 2026 the highest month at 2.
Show the numbers
Monthly 510(k) clearances under FDA product code EFB, trailing twelve months
MonthClearances
November 20250
December 20250
January 20262
February 20260
March 20260
April 20260
May 20260
June 20260
July 20260
August 20260
September 20261
October 20260