Lydall, Inc. (Unifrax LLC)
自動車および産業分野向けの特殊ろ過および熱製品。
Lydall, Inc. は現在 Unifrax LLC の一部であり、自動車、産業、医療分野向けの特殊ろ過製品および熱管理製品のメーカーです。同社のパフォーマンス マテリアルズ部門では、特殊ろ過媒体、成形繊維断熱材、および自動車の熱保護シールドを製造しています。同社のサーマル製品部門は工業用濾過製品と騒音減衰製品を供給しています。 Lydall は、世界中の自動車 OEM、工業メーカー、空気および液体の濾過システム ビルダーにサービスを提供しています。
- Type
- manufacturer (our classification of the record, not a statement by the company)
- Role
- Manufacturer
- Location
- Manchester, CT, United States
- Founded
- 1879
- Website
- lydall.com
- Categories
- 産業用品, 車両部品および付属品, 医療およびヘルスケア用品
- Markets
- アメリカ合衆国, ドイツ, 中国, 日本, 韓国, フランス
What is established and what is not
No facet of this company has been investigated yet. The facts below are collected records, not an assessment: nothing here confirms manufacturing, ownership or trading status beyond what each record literally says.
Verified facts
- corporate-mail-on-domain (green), checked 2026-08-09 Mail server of the company domain
- domain-registered (green), checked 2026-08-09 Domain registry record
- web-presence-since (green), checked 2026-08-09 Internet Archive (Wayback)
- sanctions-clear (green), checked 2026-08-09 OpenSanctions
- debarment-clear (green), checked 2026-08-09 OpenSanctions
- lei-lapsed (amber), checked 2026-09-07 GLEIF global LEI register (golden copy)
- registry-id-verified (green), checked 2026-09-10 GLEIF Global LEI record
Claimed certifications, not confirmed by us
- ISO 9001, Quality Management IAF CertSearch
- IATF 16949, Automotive Quality IAF CertSearch
- ISO 14001, Environmental Management IAF CertSearch
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)