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 GermanyLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field.. FDA records under 2 spellings of its name, each linked to the record.
As of Nov 15, 2026, FDA's public records list Karl Storz and its 12 subsidiaries with 587 510(k) clearances, 92 device recalls and 1 AI-enabled device. The most recent is a 510(k) clearance dated Oct 14, 2026: KARL STORZ Flexible Video Neuro-Endoscope.
Group recordsLabelled by a language model (which subsidiaries belong to the group) from the firm's FDA names. It is not an FDA field.: 680, 13 entities
510(k) clearances: 587
Device recalls: 92
AI-enabled devices: 1
Records by Year
Drug approvals, 510(k) clearances, recalls and letters, 2017 to 2026 to date, Karl Storz and its 12 subsidiaries
How to read this
A hatched bar is a year that is not over, so its count covers only part of the year.
102017Records10
820182018Records8vs 2017−2
102019Records10vs 2018+2
2620202020Records26vs 2019+16
102021Records10vs 2020−16
1920222022Records19vs 2021+9
182023Records18vs 2022−1
2120242024Records21vs 2023+3
222025Records22vs 2024+1
1720262026 to dateRecords17
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
