Logos are each company's own site icon, matched by name through Wikidata.Company names and logos identify the companies in public FDA and registry records and do not imply endorsement.
Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field. in United StatesLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field., part of Abbott LaboratoriesLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field.. FDA records under 6 spellings of its name, each linked to the record.
As of Nov 14, 2026, FDA's public records list Abbott Vascular with 52 510(k) clearances and 42 device recalls. The most recent is a 510(k) clearance dated Jun 30, 2022: NC TREK NEO Coronary Dilatation Catheter.
510(k) clearances: 52
Device recalls: 42
Records by Year
Drug approvals, 510(k) clearances, recalls and letters, 2017 to 2026 to date
How to read this
A hatched bar is a year that is not over, so its count covers only part of the year.
72017Records7
220182018Records2vs 2017−5
42019Records4vs 2018+2
2020202020Records20vs 2019+16
02021Records0vs 2020−20
1120222022Records11vs 2021+11
02023Records0vs 2022−11
020242024Records0vs 2023+0
42025Records4vs 2024+4
020262026 to dateRecords0
Latest Records
Newest first across sources; each opens the record
Spellings are joined only when they reduce to the same name, or a reviewed source names the same company. Sharing an FDA establishment number (FEI) is not enough: contract sites make products for many firms. Facts marked AI were labelled by a language model from the firm's FDA names; everything else comes from FDA or Wikidata.How this page is built
