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.. FDA records under 3 spellings of its name, each linked to the record.
As of Nov 13, 2026, FDA's public records list AtriCure and its 1 subsidiaries with 73 510(k) clearances and 13 device recalls. The most recent is a 510(k) clearance dated Oct 21, 2026: ACHM30 AtriClip FLEX-Mini LAA Exclusion System.
Group recordsLabelled by a language model (which subsidiaries belong to the group) from the firm's FDA names. It is not an FDA field.: 86, 2 entities
510(k) clearances: 73
Device recalls: 13
Records by Year
Drug approvals, 510(k) clearances, recalls and letters, 2017 to 2026 to date, AtriCure and its 1 subsidiaries
How to read this
A hatched bar is a year that is not over, so its count covers only part of the year.
52017Records5
620182018Records6vs 2017+1
102019Records10vs 2018+4
120202020Records1vs 2019−9
32021Records3vs 2020+2
120222022Records1vs 2021−2
22023Records2vs 2022+1
620242024Records6vs 2023+4
32025Records3vs 2024−3
120262026 to dateRecords1
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
