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Lekon

FDA UDI

Class II (US FDA UDI)

by C A I Industries Corp

Identity

Trade Name
LEKON FDA UDI
Generic Name
Acupuncture needle, single-use FDA UDI
Device Name
Acupuncture needles FDA UDI
Model / Reference
NA-03-3013 FDA UDI
Description
Acupuncture needles FDA UDI

Identifiers

Primary DI / UDI-DI
00807689003465 FDA UDI
FDA Product Code
MQX FDA UDI
GMDN Term
Acupuncture needle, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
880.5580 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Acupuncture needle, single-use

Lekon by C A I Industries Corp — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Acupuncture needle, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI d1015b43-3049-47c6-9b54-b79a304d99e0 33 fields · synced Jun 8, 2026