Venture Corporation
Solutions de conception, de fabrication et de chaîne d’approvisionnement de produits technologiques.
Venture Corporation fournit des services d'industrialisation de produits, de fabrication de produits électroniques et de chaîne d'approvisionnement aux clients technologiques. Le groupe, dont le siège est à Singapour, dessert les marchés des sciences de la vie, de l'industrie, des tests et mesures, des réseaux et des technologies grand public.
- Type
- brand seeking distribution
- Location
- Singapore
- Founded
- 1989
- Website
- venture.com.sg
- Categories
- Électronique grand public, Fournitures médicales et de santé, Machines industrielles
- Markets
- Singapour, États-Unis, Allemagne, Chine
Verified facts
- domain-registered (green), checked 2026-08-10 Domain registry record
- corporate-mail-on-domain (green), checked 2026-08-10 Mail server of the company domain
- fda-registered (green), checked 2026-08-10 FDA
- fda-contract-manufacturer (green), checked 2026-08-10 FDA
- certificate-page-on-site (amber), checked 2026-08-11 Company's own certification page
- registry-activity (green), checked 1984-08-04 ACRA Information on Corporate Entities (data.gov.sg)
- lei-active (green), checked 2026-08-30 GLEIF global LEI register (golden copy)
- debarment-clear (green), checked 2026-08-10 OpenSanctions
- sanctions-clear (green), checked 2026-08-10 OpenSanctions
- registered-since (green), checked 1984-08-04 ACRA Information on Corporate Entities (data.gov.sg)
Claimed certifications
- ISO 9001, Quality Management IAF CertSearch
- ISO 13485, Medical Devices Quality IAF CertSearch
- ISO 14001, Environmental Management 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)
- Electronics for the EU need CE marking incl. RoHS substance limits, and producers must register for WEEE take-back in each member state of sale. European Commission (CE)
- Electronics for the US market need FCC equipment authorization under 47 CFR Part 15, which covers unintentional radiators such as switch-mode power supplies, not only radio devices. US FCC (Part 15)