Lydall, Inc. (Unifrax LLC)
适用于汽车和工业领域的特种过滤和热产品。
Lydall, Inc.（现属于 Unifrax LLC）是一家为汽车、工业和医疗行业提供特种过滤和热管理产品的制造商。其高性能材料部门生产特种过滤介质、模压纤维绝缘材料和汽车热防护罩；其热产品部门提供工业过滤和降噪产品。 Lydall 为全球汽车原始设备制造商、工业制造商以及空气和液体过滤系统制造商提供服务。
- 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
- 工业用品, 车辆零配件, 医疗保健用品
- Markets
- 美国, 德国, 中国, 日本, 韩国, 法国
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)