Benta Pharma Industries
Pharmaceutical and sterile medical device manufacturer present in 40+ countries since 1994.
Benta Pharma Industries manufactures enhanced pharmaceutical formulations for CNS, cardiovascular, and metabolic conditions as well as sterile medical devices including intraocular lenses and IV-administration sets. Founded in 1994 and headquartered in Lebanon with plants in Lebanon and Egypt, the Benta Group is active in over 40 countries with regional offices in Saudi Arabia, Iraq, Egypt, and France.
- Type
- manufacturer (our classification of the record, not a statement by the company)
- Role
- Manufacturer
- Location
- Beirut, Lebanon
- Founded
- 1994
- Website
- bpi.com.lb
- Categories
- Medical & Healthcare Supplies
- Markets
- Saudi Arabia, Iraq, Egypt, France, United Arab Emirates
What is established and what is not
No facet of this company has been investigated yet. The facts below are collected records, not an assessment: nothing here confirms manufacturing, ownership or trading status beyond what each record literally says.
Verified facts
- domain-registered (green), checked 2026-08-06 Domain registry record
- debarment-clear (green), checked 2026-08-06 - screened by name only: no legal entity is established for this record, so this is not a clearance OpenSanctions
- sanctions-clear (green), checked 2026-08-06 - screened by name only: no legal entity is established for this record, so this is not a clearance OpenSanctions
- corporate-mail-on-domain (green), checked 2026-08-06 Mail server of the company domain
- certificate-page-on-site (amber), checked 2026-09-18 Company's own certification page
Claimed certifications, not confirmed by us
- Good Manufacturing Practice
- ISO 9001, Quality Management IAF CertSearch
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)