Tool · 510(k)

510(k) Predicate Finder

Find potential predicate devices for your 510(k) submission. Enter a K-number to find all clearances with the same product code, a three-letter product code to browse clearances directly, or search by device name.

Product Code: MQX FDA class 2

Needle, Acupuncture, Single Use

General Hospital

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The Single-Use Acupuncture Needle is a general hospital device consisting of a sterile, single-use fine needle used for the practice of acupuncture, in which needles are inserted at specific anatomical points to produce therapeutic effects. Classified as FDA Class 2 under 21 CFR 880.5580 in the General Hospital specialty, it is 510(k)-exempt and subject to general controls. The product code is MQX.

510(k) Clearances

50+ matches
K Number
Device Name
AIK Sterile Acupuncture Needles for Single Use
Acuzone Acupuncture Needles, KSC DB Plus Acupuncture Needles
EACU, ZAGU, JOCU, EAKU, BALANCE, TEMPO, ACUZONE, SMART, PRIME, ACUSTAR, ACUKING, Myotech Dry, Red Coral Premium, Red Coral J-Type, Red Coral Natural
KM Needles (Acupuncture Needle)
SMC ACUPUNCTURE NEEDLE
CJ-TYPE: METAL HANDLE WITH GUIDE TUBE, PJ-TYPE: PLASTIC HANDLE WITH GUIDE TUBE, CB-TYPE: METAL HANDLE WITHOUT GUIDE TUBE
WOOJEON ACUPUNCTURE NEEDLE (=SERA ACUPUNCTURE NEEDLE)
BIOMATE STERILE ACUPUNCTURE NEEDLE
ACUPUNCTURE NEEDLES
JIAJIAN ACUPUNCTURE NEEDLE
HANSO ACUPUNCTURE NEEDLE
TCMNATURELMED, HEALTHCARE, BLOODCARE, BO'S ABDOMINAL
BRIO ACUPUNCTURE NEEDLES
PRECISION PRESS TACK / INTRADERM, SEVEN STAR AND ACUPUNCTURE NEEDLES; ALPHA AND FINE POINT ACUPUNCTURE NEEDLES
LYRA ACUPUNCTURE NEEDLES
ASP TITANIUM
KANGSHENG BRAND/KANGNIAN BRAND/UNILINK BRAND/HUAZHONG BRAND ACUPUNCTURE NEEDLES
SEVEN STAR NEEDLE
TEWA CJ-TYPE, PJ-TYPE, CB-TYPE AND PB-TYPE ACUPUNCTURE NEEDLES FOR SINGLE USE
STANDARD, SPECIAL, SPECIAL+, SNEEDLE B-TYPE AND SNEEDLE J-TYPE ACUPUNCTURE NEEDLES
PRESS TACK/INTRADERMAL ACUPUNCTURE NEEDLES
ACUPUNCTURE NEEDLES
C&G ACUPUNCTURE NEEDLE
ACUPUNCTURE NEEDLES
PRESS TACK NEEDLE
FACILAI VARIOUS MODELS OF SINGLE USE ACUPUNCTURE NEEDLE
DBC PRESS ACUPUNCTURE NEEDLES
NANO TECH AND SUPER NANO ACUPUNCTURE NEEDLES
SPECIAL+, S-NEEDLE J-TYPE, S-NEEDLE B-TYPE
VINCO BRAND ACUPUNCTURE NEEDLE
CARBO/OPTIMED BRAND ACUPUNCTURE NEEDLES
TAI-CHI AND MASTER ACUPUNCTURE NEEDLES
JIA CHEN ACUPUNCTURE NEEDLE, FOR SINGLE USE
MAEDA SILVER ACUPUNCTURE NEEDLE
QIZHOU ACUPUNCTURE NEEDLE
MARKNEW PRODUCTS ACUPUNCTURE NEEDLES
HOLY DRAGON BRAND ACUPUNCTURE NEEDLES
ACUGLIDE BRAND ACUPUNCTURE NEEDLES
H.M.T. ACUPUNCTURE NEEDLE
CW DISPOSABLE ACUPUNCTURE NEEDLE
HOLY DRAGON STERILE ACUPUNCTURE NEEDLE FOR SINGLE USE
HUANQIU AND SUPER (TWO BRANDS) STERILE ACUPUNCTURE NEEDLE FOR SINGLE USE
ASIA-MED ACUPUNCTURE NEEDLES, (STANDARD, SPECIAL, COMPACT, APEX)
BW ACUPUNCTURE NEEDLES
MAC ACUPUNCTURE NEEDLE
MAEDA NEW NEEDLE DISPOSABLE
HOLY DRAGON ACUPUNCTURE NEEDLES
TAI-CHI ACUPUNCTURE NEEDLES
TIANXIE
SHENLING ACUPUNCTURE NEEDLES

What is a Predicate Device?

A predicate device is a legally marketed device that a new 510(k) applicant uses to demonstrate substantial equivalence. The FDA's 510(k) pathway requires manufacturers to show that their device has the same intended use and similar technological characteristics as one or more predicate devices already cleared for commercial distribution.

Finding the right predicate is a critical step in 510(k) strategy. Manufacturers typically search for cleared devices with the same FDA product code, which groups devices by their intended use and regulatory classification. This tool helps you identify potential predicates by browsing all clearances within a product code.

Note that predicate devices must be legally marketed — they cannot be devices that were cleared but never commercialized, or devices subject to a mandatory recall. The determination of substantial equivalence considers intended use, technological characteristics, and performance data.

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