FARMTECH CO., LTD.

FDA Device Registration & Listing · Icheon-si Gyeonggi, KR · Registration 3015272250

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
3015272250
FEI Number
3015272250
Entity Name
FARMTECH CO., LTD.
City/State/Country
Icheon-si Gyeonggi, KR
Establishment Address
65-116, Cheongbaengni-ro 697beon-gil, Baeksa-myeon, Icheon-si Gyeonggi 17313, KR
Establishment Type(s)
Manufacture Medical Device for Another Party (Contract Manufacturer),Manufacture Medical Device
Owner / Operator
Farmtech Co., Ltd. (Owner Number: 10060145)
Owner / Operator Contact Address
65-116, Cheongbaengni-ro 697beon-gil, Baeksa-myeon, Icheon-si, KR-41 17313, KR
Initial Importer Flag
N
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
IMD Pack, Hot Or Cold, Disposable Physical Medicine Class 1 890.5710 2019-04-03

Official Correspondent

No official correspondent registered.

US Agent Details

Jinwook Kim Email: jinwook.kim@gfvcorp.com Phone: (213) 3923336

Related Public Records

Same Entity

Farmtech Co., Ltd.
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
K880871 John Wagner Associates, Inc. GRABBER WARM PACK/MINI MINI HEATER/FOOT HEATER 1988-05-20

Related Recall Records

Recall ID Recalling Firm Recall Class Product Description
Z-0505-2022 Philips North America Llc 1
Infa-Therm Transport Mattress, Reference Number 989805616831 1015
Z-0506-2022 Philips North America Llc 1
Infant Heel Warmers w/strap, Reference # 989805603201 1223

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3015272250. Last updated year: 2026. Please use registration number 3015272250 when referencing this establishment in official correspondence.
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