UFP Technologies, Inc.
Soluciones personalizadas de espuma, fibra y embalaje para los sectores médico e industrial.
UFP Technologies es un diseñador y fabricante de embalajes, componentes y productos especiales innovadores fabricados con espuma, fibra y materiales de conversión especiales. Su segmento médico produce sistemas de posicionamiento quirúrgico a base de espuma, envases médicos especializados y componentes compatibles con salas blancas para fabricantes de dispositivos. La empresa también suministra espuma de poliuretano personalizada y embalajes troquelados para aplicaciones industriales, aeroespaciales y de protección de productos de consumo.
- Type
- brand seeking distribution
- Location
- Newburyport, MA, United States
- Founded
- 1963
- Website
- ufpt.com
- Categories
- Embalaje y suministros de impresión, Suministros médicos y sanitarios, Suministros industriales
- Markets
- Estados Unidos, Canadá, Alemania, Reino Unido
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 2026-08-23 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
Claimed certifications
- ISO 9001, Quality Management IAF CertSearch
- ISO 13485, Medical Devices Quality IAF CertSearch
- FDA Registered FDA Establishment Registration
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)