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 14, 2026, FDA's public records list Glidewell and its 2 subsidiaries with 60 510(k) clearances and 4 device recalls. The most recent is a 510(k) clearance dated Aug 27, 2026: Glidewell™ Denture Base Resin.
Group recordsLabelled by a language model (which subsidiaries belong to the group) from the firm's FDA names. It is not an FDA field.: 64, 3 entities
510(k) clearances: 60
Device recalls: 4
Records by Year
Drug approvals, 510(k) clearances, recalls and letters, 2017 to 2026 to date, Glidewell 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.
12017Records1
020182018Records0vs 2017−1
32019Records3vs 2018+3
120202020Records1vs 2019−2
32021Records3vs 2020+2
420222022Records4vs 2021+1
62023Records6vs 2022+2
720242024Records7vs 2023+1
72025Records7vs 2024+0
420262026 to dateRecords4
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
