HLL Lifecare
Government of India enterprise, healthcare products reaching the last mile.
HLL Lifecare (Hindustan Latex Limited) is a Government of India Mini-Ratna enterprise headquartered in Thiruvananthapuram, manufacturing contraceptives, surgical gloves, condoms, IUDs, sanitary napkins and diagnostics. It supplies to national health programmes and exports to over 130 countries across Africa, Asia and the Middle East.
- Type
- Manufacturer
- Location
- Thiruvananthapuram, India
- Founded
- 1966
- Website
- lifecarehll.com
- Categories
- Medical & Healthcare Supplies, Personal Care
- Markets
- India, United Arab Emirates, Nigeria, Kenya, Bangladesh
Verified facts
- corporate-mail-on-domain (green), checked 2026-08-08 Mail server of the company domain
- domain-registered (green), checked 2026-08-08 Domain registry record
- fda-registered (green), checked 2026-08-08 FDA
- debarment-clear (green), checked 2026-08-08 OpenSanctions
- sanctions-clear (green), checked 2026-08-08 OpenSanctions
- standards-mark-certified (green), checked 2026-08-21 Bureau of Indian Standards (BIS), all-India first licence report (ISI Standard Mark)
- export-registered (green), checked 2026-08-21 Pharmexcil member directory (Pharmaceuticals Export Promotion Council of India, Ministry of Commerce)
- registered-manufacturer (green), checked 2026-08-21 Pharmexcil member directory (Pharmaceuticals Export Promotion Council of India, Ministry of Commerce)
- lei-active (green), checked 2026-08-23 GLEIF global LEI register (golden copy)
Claimed certifications
- Good Manufacturing Practice
- ISO 9001, Quality Management IAF CertSearch
- ISO 13485, Medical Devices Quality IAF CertSearch
- FDA Registered FDA Establishment Registration
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)