Synthite Industries Ltd
Synthite Industries is the world's largest producer of value-added spice extracts and natural foo…
Synthite Industries is the world's largest producer of value-added spice extracts and natural food colorants, processing over 25,000 metric tonnes of raw spices annually at its Kerala and Karnataka plants. Its portfolio spans oleoresins, essential oils, spray-dried powders, encapsulated flavors and marigold-derived lutein for nutraceuticals. Wholesale buyers in the food, pharma and cosmetic sectors rely on Synthite for traceable supply chains, 400+ product variants and regulatory support covering EU, US and Japanese markets.
- Type
- Manufacturer
- Location
- Kochi, India
- Founded
- 1972
- Website
- synthite.com
- Categories
- Specialty & Gourmet Food, Medical & Healthcare Supplies
- Markets
- United States, Germany, Japan, United Kingdom, Netherlands
Verified facts
- domain-registered (green), checked 2026-08-09 Domain registry record
- standards-mark-certified (green), checked 2026-08-16 EAEU unified register of certificates and declarations
- sanctions-clear (green), checked 2026-08-09 OpenSanctions
- corporate-mail-on-domain (green), checked 2026-08-09 Mail server of the company domain
- debarment-clear (green), checked 2026-08-09 OpenSanctions
Claimed certifications
- ISO 9001, Quality Management IAF CertSearch
- ISO 22000, Food Safety IAF CertSearch
- HACCP
- Halal Certified
- Kosher Certified
- USDA Organic USDA Organic INTEGRITY
- EAC mark (EAEU conformity) EAEU unified register of certificates and declarations
Import rules for these goods
- EU imports of food of animal origin and many other food categories must be pre-notified in TRACES and enter through border control posts. European Commission (TRACES)
- US imports require the foreign facility to be FDA-registered and the importer to run a Foreign Supplier Verification Program (FSVP). US FDA
- 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)