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.. FDA files no records under this name; these are its 2 companies' records, each linked to the record.
As of Nov 13, 2026, FDA's public records list Straumann Group and its 2 subsidiaries with 75 510(k) clearances and 33 device recalls. The most recent is a device recall dated Oct 27, 2014: Drill set long, drill stop compatible for 4.8mm diameter implant, Article Number 040.447….
Group recordsLabelled by a language model (which subsidiaries belong to the group) from the firm's FDA names. It is not an FDA field.: 108, 3 entities
510(k) clearances: 75
Device recalls: 33
Records by Year
Drug approvals, 510(k) clearances, recalls and letters, 2017 to 2026 to date, Straumann Group and its 2 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
820182018Records8vs 2017+3
12019Records1vs 2018−7
220202020Records2vs 2019+1
42021Records4vs 2020+2
220222022Records2vs 2021−2
02023Records0vs 2022−2
120242024Records1vs 2023+1
62025Records6vs 2024+5
820262026 to dateRecords8
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
