510(K) CLEARANCES 75 ▼9RECALLS POSTED 26 ▼13CLASS I 2 ▼4PMA DECISIONS 54 ▲7WEEK ENDING / FDA DATA AS OF
Medical Device
ManufacturingTHE TRADE PAPER OF THE FACTORY FLOOR
SUBSCRIBE / SIGN IN
K021904Substantially Equivalent

Maeda Silver Acupuncture Needle

Maeda Toyokichi Shoten, Crofton MD / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K021904 is the FDA 510(k) clearance record for MAEDA SILVER ACUPUNCTURE NEEDLE, a class II device, cleared for Maeda Toyokichi Shoten on under FDA product code MQX (Needle, Acupuncture, Single Use). FDA records list 2 510(k) clearances for Maeda Toyokichi Shoten, from to . As of , FDA records show no recalls naming K021904.

Clearance record

Decision date
Received
(65 days to decision)
Product code
MQX Needle, Acupuncture, Single Use
Regulation
21 CFR 880.5580
Device class
Class II
Review panel
General Hospital
Applicant
Maeda Toyokichi Shoten P.O. Box 4341, Crofton MD
510(k) summary
Statement
Third party review
No

Clearances, product code MQX

Trailing 12 months

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

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