MKT Co., Ltd.
Company-provided description, not an official-source fact. Certifications, capacities, years and market positions stated in it are the company's own claims until a record below confirms them.
消防設備メーカー
MKT は、2026 年韓国消防安全エキスポの公式ディレクトリに掲載されており、企業の直接 Web サイトも開設されています。企業のホームページには、製造および防火製品の証拠が含まれています。
- Type
- manufacturer (our classification of the record, not a statement by the company)
- Role
- Manufacturer (official record)
- Location
- Incheon, South Korea
- Founded
- 2006 (from our catalogue record; not confirmed by the company or by a state register)
- Website
- https://komkt.co.kr
- Categories
- 医療およびヘルスケア用品
- Markets
- 韓国
Listed in a source registry
Fire and Safety EXPO Korea 2026 directory
What is established and what is not
No researcher review has been written for this company yet. 1 official record from 1 official source is on file. 2 other entries are not official records: our own technical checks and searches, open directory listings, our inferences or the company's own statements. Everything is listed below with its evidence type: each entry confirms only what it literally says; none of them is a review. The manufacturing role above rests on the official records listed below, and only as far as each literally goes: a facility registration or licence is not an observation of current production. Nothing here confirms ownership or trading status beyond what each record literally says.
Facts on file, each with its evidence type
- Business email on the company's own domain (record type: corporate-mail-on-domain) [our own observation, not an official record; status green] Shows the domain runs its own email rather than a free mailbox. It describes the domain, not who owns it. checked 2026-09-06. Mail server of the company domain
- Registered as a manufacturer (record type: registered-manufacturer) [official record; status green] Its own declared activity in the register covers making these goods. effective since 2024-12-31. Korea Industrial Complex Corporation registered-factory list (data.go.kr)
- First recorded on the web archive (record type: web-presence-since) [our own observation, not an official record; status green] The company website was already online in 2012. Shows a web archive saw a page at this address on that date. It does not show who ran the site then. checked 2026-09-06. Internet Archive (Wayback)
Import rules for these goods
- Medical devices sold in the EU must carry CE marking under the Medical Device Regulation (EU) 2017/745, with a conformity assessment matched to the device risk class. European Commission (MDR)
- For the US market, the maker must have an FDA device establishment registration and product listing; most instruments also need 510(k) premarket clearance. US FDA (devices)
Check independently
Before a first order, ask for the legal entity's registration number and country, then check it in the official register.