AYBARION TRADECompany profile · US
St. Jude Medical, Atrial Fibrillation Division, Inc.
Inc. in Minnetonka, United States, from the official register data of openFDA Device Registration & Listing, with official trade evidence and its GLEIF group.
Company identity
| Legal name | St. Jude Medical, Atrial Fibrillation Division, Inc. |
|---|---|
| Country | United States |
| City | Minnetonka |
| Registry ID | 2182269 (openFDA Device Registration & Listing) |
| Status | Active |
| Legal form | Inc. |
| Sector | NACE Rev.2 section C: Manufacturing |
| Founded | 1974 |
| LEI | 549300HQBF4CV2K2EL67 |
Copied from the register record us-fda:2182269 of openFDA Device Registration & Listing, snapshot 2026-09-28. No street address, people or contact details are shown.
Official trade evidence
2 official records in 1 kind name this company:
- Foreign medical device suppliers (FDA registration): 2 records, 8 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 | 1000139754 | 4 | exact legal name | |
| Foreign medical device suppliers (FDA registration) | FDA device establishment registration: foreign manufacturers and their US initial importers | 2182269 | 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: ISSUED, next renewal 2027-10-01.
| Entity | Country | Relation | LEI |
|---|---|---|---|
| ABBOTT LABORATORIES | United States | Ultimate parent | HQD377W2YR662HK5JX27 |
Source: GLEIF relationship records (CC0). Entities in countries without company data are not listed.
Data Passport
- openFDA Device Registration & Listing: U.S. Food and Drug Administration (Official establishment list (FDA)). Licence: CC0 1.0. Snapshot 2026-09-28. Record ID: us-fda:2182269. Source
- GLEIF Golden Copy: LEI and relationship records: Global Legal Entity Identifier Foundation. Licence: CC0 1.0. Record: LEI 549300HQBF4CV2K2EL67. 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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