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 LiechtensteinLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field.. FDA records under 5 spellings of its name, each linked to the record.
As of Nov 15, 2026, FDA's public records list Ivoclar Vivadent and its 3 subsidiaries with 111 510(k) clearances and 44 device recalls. The most recent is a 510(k) clearance dated Jul 1, 2026: Tetric plus Fill;Tetric plus Flow.
Group recordsLabelled by a language model (which subsidiaries belong to the group) from the firm's FDA names. It is not an FDA field.: 155, 4 entities
510(k) clearances: 111
Device recalls: 44
Records by Year
Drug approvals, 510(k) clearances, recalls and letters, 2017 to 2026 to date, Ivoclar Vivadent and its 3 subsidiaries
How to read this
A hatched bar is a year that is not over, so its count covers only part of the year.
12017Records1
520182018Records5vs 2017+4
52019Records5vs 2018+0
620202020Records6vs 2019+1
12021Records1vs 2020−5
120222022Records1vs 2021+0
02023Records0vs 2022−1
820242024Records8vs 2023+8
02025Records0vs 2024−8
320262026 to dateRecords3
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
