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 its name, each linked to the record.
As of Nov 14, 2026, FDA's public records list DJO Global and its 3 subsidiaries with 100 device recalls and 97 510(k) clearances. The most recent is a 510(k) clearance dated Oct 2, 2026: AltiVate Reverse® Glenosphere with RAVN™ Technology.
Group recordsLabelled by a language model (which subsidiaries belong to the group) from the firm's FDA names. It is not an FDA field.: 197, 4 entities
Device recalls: 100
510(k) clearances: 97
Records by Year
Drug approvals, 510(k) clearances, recalls and letters, 2017 to 2026 to date, DJO Global 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.
192017Records19
1420182018Records14vs 2017−5
62019Records6vs 2018−8
1120202020Records11vs 2019+5
62021Records6vs 2020−5
620222022Records6vs 2021+0
192023Records19vs 2022+13
420242024Records4vs 2023−15
232025Records23vs 2024+19
920262026 to dateRecords9
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
