ENGEL Austria GmbH
ENGEL is Europe's largest injection moulding machine manufacturer and a global technology leader…
ENGEL is Europe's largest injection moulding machine manufacturer and a global technology leader in plastics processing equipment. The Schwertberg factory produces the tie-bar-less victory series and large two-platen duo series machines from 28 to 5,500 tonnes clamping force. Customers include automotive Tier 1 suppliers, medical device manufacturers, and packaging companies in 85 countries. Full-line automation, tooling, and IIoT solutions available alongside machinery.
- Type
- Manufacturer
- Location
- Schwertberg, Austria
- Founded
- 1945
- Website
- engelglobal.com
- Categories
- Packaging & Printing Supplies, Personal Care, Medical & Healthcare Supplies
- Markets
- Germany, United States, China, Japan, United Kingdom
Verified facts
- domain-registered (green), checked 2026-08-08 Domain registry record
- standards-mark-certified (green), checked 2026-08-16 EAEU unified register of certificates and declarations
- lei-active (green), checked 2026-08-23 GLEIF global LEI register (golden copy)
- corporate-mail-on-domain (green), checked 2026-08-08 Mail server of the company domain
- sanctions-clear (green), checked 2026-08-08 OpenSanctions
- debarment-clear (green), checked 2026-08-08 OpenSanctions
Claimed certifications
- ISO 9001, Quality Management IAF CertSearch
- EAC mark (EAEU conformity) EAEU unified register of certificates and declarations
Import rules for these goods
- Cosmetic products must be notified in the EU Cosmetic Products Notification Portal (CPNP) before being placed on the EU market. European Commission (CPNP)
- For the US market, MoCRA requires cosmetic facility registration and product listing with the FDA. US FDA (MoCRA)
- 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)