KORSMET US INC

FDA Device Registration & Listing · City of Industry, CA, US · Registration 3032245645

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
3032245645
FEI Number
3032245645
Entity Name
KORSMET US INC
City/State/Country
City of Industry, CA, US
Establishment Address
17709 VALLEY BLVD, City of Industry, CA 91744, US
Establishment Type(s)
Repack or Relabel Medical Device
Owner / Operator
KORSMET US INC (Owner Number: 10094159)
Owner / Operator Contact Address
17709 VALLEY BLVD, City of Industry, CA 91744, US
Initial Importer Flag
Y
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

No proprietary names listed under this establishment.

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
EFW Toothbrush, Manual Dental Class 1 872.6855 2025-12-08
KGX Tape And Bandage, Adhesive General Hospital Class 1 880.5240 2026-01-13
NRC Pad, Menstrual, Scented, Scented-Deodorized Made Of Common Cellulosic & Synthetic Material W/Established Safety Profile Obstetrics/Gynecology Class 1 884.5425 2026-01-13
HHD Pad, Menstrual, Unscented Obstetrics/Gynecology Class 1 884.5435 2025-11-17

Official Correspondent

QIAN Peng

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

KORSMET US INC
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

Related 510(k) Records

510(k) Number Applicant Device Name Decision Date
K973236 Procter & Gamble Co. CREST TOOTHBRUSH WITH MICROSHIELD 1998-03-11
K843874 Beiersdorf, Inc. LEUKOPOR SURGICAL TAPE 1985-02-21
K915446 Sun Glitz Corp. STRETCH WRAP 1992-05-06
K833120 Acme United Corp. ONE TIME COMPOUND BENZOIN TINCTURE- 1983-12-29
K870091 Avery Intl. IV SECUREMENT DEVICE USING PCCE THERMO. FILM 1987-02-04

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3032245645. Last updated year: 2026. Please use registration number 3032245645 when referencing this establishment in official correspondence.
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