UFP Technologies, Inc.
Solutions personnalisées en mousse, fibre et emballage pour les secteurs médical et industriel.
UFP Technologies est un concepteur et fabricant d'emballages, de composants et de produits spécialisés innovants fabriqués à partir de mousse, de fibres et de matériaux de conversion spécialisés. Son secteur médical produit des systèmes de positionnement chirurgical à base de mousse, des emballages médicaux spécialisés et des composants compatibles avec les salles blanches pour les fabricants d'appareils. La société fournit également de la mousse de polyuréthane personnalisée et des emballages découpés pour les applications industrielles, aérospatiales et de protection des produits de consommation.
- Type
- manufacturer (our classification of the record, not a statement by the company)
- Role
- Manufacturer
- Location
- Newburyport, MA, United States
- Founded
- 1963
- Website
- ufpt.com
- Categories
- Emballage et fournitures d'impression, Fournitures médicales et de santé, Fournitures industrielles
- Markets
- États-Unis, Canada, Allemagne, Royaume-Uni
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 2026-08-10 Mail server of the company domain
- debarment-clear (green), checked 2026-08-10 OpenSanctions
- certificate-page-on-site (amber), checked 2026-08-11 Company's own certification page
- lei-lapsed (amber), checked 2026-09-07 GLEIF global LEI register (golden copy)
- domain-registered (green), checked 2026-08-10 Domain registry record
- fda-registered (green), checked 2026-08-10 FDA
- fda-contract-manufacturer (green), checked 2026-08-10 FDA
- sanctions-clear (green), checked 2026-08-10 OpenSanctions
- registry-id-verified (green), checked 2026-09-10 GLEIF Global LEI record
Claimed certifications, not confirmed by us
- ISO 9001, Quality Management IAF CertSearch
- ISO 13485, Medical Devices Quality 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)
- If the goods are paper, board or printed products, EU imports fall under the Deforestation Regulation (EUDR) due-diligence regime; packaging machinery itself does not. European Commission (EUDR)