KM SUPPLIES

FDA Device Registration & Listing · Los Angeles, CA, US · Registration 3008400688

Public Record Device Listing Expiry Year: 2026 This page presents structured fields from public FDA datasets.

Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source
FDA Device Registration & Listing
Record Type
Device registration/listing
Registration Number
3008400688
FEI Number
3008400688
Entity Name
KM SUPPLIES
City/State/Country
Los Angeles, CA, US
Establishment Address
1132 Crenshaw Blvd, Los Angeles, CA 90019, US
Establishment Type(s)
Develop Specifications But Do Not Manufacture At This Facility
Owner / Operator
KM Supplies (Owner Number: 10040673)
Owner / Operator Contact Address
1132 Crenshaw Blvd., Los Angeles, CA 90019, US
Initial Importer Flag
Y
Expiration Date (Year)
2026
510(k) Number
K162566
PMA Number
N/A

All Registered Proprietary Names

KMA Acupuncture Needle, Single Use

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
MQX Needle, Acupuncture, Single Use General Hospital Class 2 880.5580 2024-02-22

Official Correspondent

Peter Yi

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

KM Supplies
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3008400688. Last updated year: 2026. Please use registration number 3008400688 when referencing this establishment in official correspondence.
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