Sonoco Products Company
Diversified global packaging solutions for consumer and industrial markets.
Sonoco Products Company is a global provider of diversified consumer and industrial packaging solutions, operating more than 300 manufacturing facilities in over 30 countries. The company produces composite cans, paperboard tubes and cores, rigid and flexible plastic containers, specialty packaging for healthcare products, and global packaging services. Sonoco's healthcare packaging division manufactures medical pouches, blister packs, and specialty materials for medical device and pharmaceutical customers, while its consumer packaging segment supplies cans, labels, and rigid paper containers to food and personal care brands.
- Type
- Manufacturer
- Location
- Hartsville, SC, United States
- Founded
- 1899
- Website
- sonoco.com
- Categories
- Packaging & Printing Supplies, Industrial Supplies, Medical & Healthcare Supplies
- Markets
- United States, Canada, Mexico, Germany, United Kingdom, Brazil, China
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 2026-08-02 Internet Archive (Wayback)
- lei-active (green), checked 2026-08-23 GLEIF global LEI register (golden copy)
- cert-fsc (amber), checked 2026-08-16 FSC certificate database (search.fsc.org)
- debarment-clear (green), checked 2026-08-09 OpenSanctions
- sanctions-clear (green), checked 2026-08-09 OpenSanctions
Claimed certifications
- ISO 9001, Quality Management IAF CertSearch
- ISO 14001, Environmental Management IAF CertSearch
- ISO 45001, Occupational Safety IAF CertSearch
- FSC Certified FSC Public Search
- BRCGS Certification BRCGS Directory
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)