Lydall, Inc. (Unifrax LLC)
Otomotiv ve endüstriyel sektörlere yönelik özel filtreleme ve termal ürünler.
Artık Unifrax LLC'nin bir parçası olan Lydall, Inc., otomotiv, endüstriyel ve medikal sektörlere yönelik özel filtreleme ve termal yönetim ürünleri üreticisidir. Performans Malzemeleri segmenti, özel filtreleme ortamları, kalıplanmış fiber izolasyon ve termal olarak koruyucu otomotiv kalkanları üretiyor; Termal Ürünler segmenti, endüstriyel filtreleme ve gürültü sönümleme ürünleri tedarik etmektedir. Lydall, dünya çapında otomotiv OEM'lerine, endüstriyel üreticilere ve hava ve sıvı filtreleme sistemi üreticilerine hizmet vermektedir.
- 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
- Endüstriyel Malzemeler, Araç Parçaları ve Aksesuarları, Tıbbi ve Sağlık Malzemeleri
- Markets
- Amerika Birleşik Devletleri, Almanya, Çin, Japonya, Güney Kore, Fransa
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)