510(K) CLEARANCES 67 ▼8RECALLS POSTED 26CLASS I 2PMA DECISIONS 40 ▼14WEEK ENDING / FDA DATA AS OF
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K002411Substantially Equivalent

Shenling Acupuncture Needles

Shenling Medical Device Co., Ltd., Los Angeles CA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K002411 is the FDA 510(k) clearance record for SHENLING ACUPUNCTURE NEEDLES, a class II device, cleared for Shenling Medical Device Co., Ltd. on under FDA product code MQX (Needle, Acupuncture, Single Use). FDA records list one 510(k) clearance for Shenling Medical Device Co., Ltd. As of , FDA records show no recalls naming K002411.

Clearance record

Decision date
Received
(127 days to decision)
Product code
MQX Needle, Acupuncture, Single Use
Regulation
21 CFR 880.5580
Device class
Class II
Review panel
General Hospital
Applicant
Shenling Medical Device Co., Ltd. 1800 Century Park E. Suite 600, Los Angeles CA
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