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 15, 2026, FDA's public records list Carl Zeiss AG and its 11 subsidiaries with 148 510(k) clearances, 29 device recalls and 2 AI-enabled devices. The most recent is a 510(k) clearance dated Oct 15, 2026: MICOR 700 System (N/A); MICOR 700 Extractor (FG-50621).
Group recordsLabelled by a language model (which subsidiaries belong to the group) from the firm's FDA names. It is not an FDA field.: 179, 12 entities
510(k) clearances: 148
Device recalls: 29
AI-enabled devices: 2
Records by Year
Drug approvals, 510(k) clearances, recalls and letters, 2017 to 2026 to date, Carl Zeiss AG and its 11 subsidiaries
How to read this
A hatched bar is a year that is not over, so its count covers only part of the year.
82017Records8
1120182018Records11vs 2017+3
72019Records7vs 2018−4
720202020Records7vs 2019+0
32021Records3vs 2020−4
820222022Records8vs 2021+5
92023Records9vs 2022+1
420242024Records4vs 2023−5
42025Records4vs 2024+0
520262026 to dateRecords5
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
