AYBARION TRADECompany profile · US
LANSINOH LABORATORIES INC
Inc. in United States, from the official register data of ANVISA open data: medical device manufacturing sites, API manufacturers and GMP certified plants (foreign), with official trade evidence and its GLEIF group.
Company identity
| Legal name | LANSINOH LABORATORIES INC |
|---|---|
| Country | United States |
| Status | Active |
| Legal form | Inc. |
| Sector | NACE Rev.2 section C: Manufacturing |
| Founded | 2000 |
| Website | lansinoh.com |
| LEI | 549300AUORSEFZX83F40 |
Copied from the register record br-anvisa-foreign:6903 of ANVISA open data: medical device manufacturing sites, API manufacturers and GMP certified plants (foreign). No street address, people or contact details are shown.
Official trade evidence
1 official record in 1 kind name this company:
- Foreign medical device suppliers (FDA registration): 1 record, 4 suppliers
| Kind | Source | Record | Period | Count | Matched by |
|---|---|---|---|---|---|
| Foreign medical device suppliers (FDA registration) | FDA device establishment registration: foreign manufacturers and their US initial importers | 3022898 | 4 | exact legal name |
Records of official open datasets, matched by registry number or by the exact legal name in the same country. Each source link opens the publisher's dataset.
Corporate group (GLEIF)
LEI registration status: LAPSED, next renewal 2018-03-30.
GLEIF reports no parent or subsidiary for this LEI.
Source: GLEIF relationship records (CC0). Entities in countries without company data are not listed.
Data Passport
- ANVISA open data: medical device manufacturing sites, API manufacturers and GMP certified plants (foreign): Agência Nacional de Vigilância Sanitária (ANVISA) (Official foreign manufacturer list (ANVISA)). Licence: CC BY (dados.gov.br). Attribution: "ANVISA, Dados Abertos (dados.anvisa.gov.br), CC BY". Record ID: br-anvisa-foreign:6903.
- GLEIF Golden Copy: LEI and relationship records: Global Legal Entity Identifier Foundation. Licence: CC0 1.0. Record: LEI 549300AUORSEFZX83F40. Source
- FDA device establishment registration: foreign manufacturers and their US initial importers: U.S. Food and Drug Administration. Licence: U.S. Government work (public domain). Period 2026-10-19 to 2026-10-19. Source
- Method: identity fields are copied from the register record as published (legal name, country, city, registry ID, status, legal form, activity code, founded year, website domain, LEI). Official trade records are matched by registry number or exact legal name in the same country; group relations are GLEIF relationship records. Street addresses, people and contact details are never stored or shown.
Public company pages cover legal entities from registers published under CC0, CC BY, the Open Government Licence, the Licence Ouverte or in the public domain. Sole traders are never shown. Directory built 2026-10-30. More in our methodology and the public company pages policy.
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