Lydall, Inc. (Unifrax LLC)
Speciale filtratie- en thermische producten voor de automobiel- en industriële sector.
Lydall, Inc., nu onderdeel van Unifrax LLC, is een fabrikant van speciale filtratie- en thermische beheerproducten voor de automobiel-, industriële en medische sector. Het Performance Materials-segment produceert speciale filtratiemedia, gegoten vezelisolatie en thermisch beschermende autoschilden; het segment Thermal Products levert industriële filtratie- en geluidsdempende producten. Lydall bedient OEM's uit de auto-industrie, industriële fabrikanten en bouwers van lucht- en vloeistoffiltratiesystemen over de hele wereld.
- 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
- Industriële benodigdheden, Voertuigonderdelen en accessoires, Medische en gezondheidszorgbenodigdheden
- Markets
- Verenigde Staten, Duitsland, China, Japan, Zuid-Korea, Frankrijk
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)