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 15, 2026, FDA's public records list Hollister Incorporated and its 3 subsidiaries with 112 510(k) clearances and 9 device recalls. The most recent is a device recall dated Jul 14, 2026: Onli 17cm Hydrophilic Urethral Intermittent Catheter, labeled as: 1) 82081 Ch08-17 On….
Group recordsLabelled by a language model (which subsidiaries belong to the group) from the firm's FDA names. It is not an FDA field.: 121, 4 entities
510(k) clearances: 112
Device recalls: 9
Records by Year
Drug approvals, 510(k) clearances, recalls and letters, 2017 to 2026 to date, Hollister Incorporated 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
320182018Records3vs 2017+2
22019Records2vs 2018−1
020202020Records0vs 2019−2
22021Records2vs 2020+2
420222022Records4vs 2021+2
02023Records0vs 2022−4
120242024Records1vs 2023+1
52025Records5vs 2024+4
220262026 to dateRecords2
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
