Lydall, Inc. (Unifrax LLC)
자동차 및 산업 부문을 위한 특수 여과 및 열 제품.
현재 Unifrax LLC의 일부인 Lydall, Inc.는 자동차, 산업 및 의료 부문을 위한 특수 여과 및 열 관리 제품 제조업체입니다. Performance Materials 부문은 특수 여과 매체, 성형 섬유 단열재 및 열 보호 자동차 쉴드를 생산합니다. 열 제품 부문은 산업용 여과 및 소음 감소 제품을 공급합니다. Lydall은 전 세계적으로 자동차 OEM, 산업 제조업체, 공기 및 액체 여과 시스템 빌더에 서비스를 제공합니다.
- 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
- 산업용품, 차량 부품 및 액세서리, 의료 및 건강 관리 용품
- Markets
- 미국, 독일, 중국, 일본, 대한민국, 프랑스
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)