Lydall, Inc. (Unifrax LLC)
Filtragem especializada e produtos térmicos para os setores automotivo e industrial.
Lydall, Inc., agora parte da Unifrax LLC, é fabricante de produtos especiais de filtragem e gerenciamento térmico para os setores automotivo, industrial e médico. Seu segmento de Performance Materials produz meios de filtração especiais, isolamento de fibra moldada e blindagens automotivas de proteção térmica; seu segmento de Produtos Térmicos fornece produtos de filtragem industrial e amortecimento de ruído. Lydall atende OEMs automotivos, fabricantes industriais e construtores de sistemas de filtragem de ar e líquidos em todo o mundo.
- 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
- Suprimentos industriais, Peças e acessórios para veículos, Suprimentos médicos e de saúde
- Markets
- Estados Unidos, Alemanha, China, Japão, Coreia do Sul, França
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)