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
K111169Substantially Equivalent

Protraction Face Mask, Reverse Pull Face Mask Model Km-Pvs, Km-Pis, Km-Pvm, Km-Pim, Model Km-Fms, Km-Fml, Km-Fmf

Kwang Myung Daicom Ltd., Fullerton CA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K111169 is the FDA 510(k) clearance record for PROTRACTION FACE MASK, REVERSE PULL FACE MASK MODEL KM-PVS, KM-PIS, KM-PVM, KM-PIM, MODEL KM-FMS, KM-FML, KM-FMF, a class II device, cleared for Kwang Myung Daicom, Inc. on under FDA product code DZB (Headgear, Extraoral, Orthodontic). FDA records list one 510(k) clearance for Kwang Myung Daicom, Inc. As of , FDA records show no recalls naming K111169.

Clearance record

Decision date
Received
(160 days to decision)
Product code
DZB Headgear, Extraoral, Orthodontic
Regulation
21 CFR 872.5500
Device class
Class II
Review panel
Dental
Applicant
Kwang Myung Daicom, Inc. 951 St.Arbuck St., Fullerton CA
510(k) summary
Statement
Third party review
No

Clearances, product code DZB

Trailing 12 months

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

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