510(K) CLEARANCES 75 ▼9RECALLS POSTED 26 ▼13CLASS I 2 ▼4PMA DECISIONS 54 ▲7WEEK ENDING / FDA DATA AS OF
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K052731Substantially Equivalent

Kangsheng Brand/kangnian Brand/unilink Brand/huazhong Brand Acupuncture Needles

Daxin LI, San Marino CA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K052731 is the FDA 510(k) clearance record for KANGSHENG BRAND/KANGNIAN BRAND/UNILINK BRAND/HUAZHONG BRAND ACUPUNCTURE NEEDLES, a class II device, cleared for Daxin LI on under FDA product code MQX (Needle, Acupuncture, Single Use). FDA records list one 510(k) clearance for Daxin LI. As of , FDA records show no recalls naming K052731.

Clearance record

Decision date
Received
(125 days to decision)
Product code
MQX Needle, Acupuncture, Single Use
Regulation
21 CFR 880.5580
Device class
Class II
Review panel
General Hospital
Applicant
Daxin LI 2600 Mission St., San Marino CA
510(k) summary
Summary PDF
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