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 4 spellings of its name, each linked to the record.
As of Nov 15, 2026, FDA's public records list Dornier Medtech America with 47 510(k) clearances and 1 device recall. The most recent is a 510(k) clearance dated Dec 5, 2025: Dornier Bi-Polar Electrode BIP12CLM Bipolar 12° Medium Cutting Loop 24 Fr Electrode-Ster….
510(k) clearances: 47
Device recalls: 1
Records by Year
Drug approvals, 510(k) clearances, recalls and letters, 2017 to 2026 to date
How to read this
A hatched bar is a year that is not over, so its count covers only part of the year.
22017Records2
120182018Records1vs 2017−1
42019Records4vs 2018+3
220202020Records2vs 2019−2
12021Records1vs 2020−1
220222022Records2vs 2021+1
12023Records1vs 2022−1
120242024Records1vs 2023+0
22025Records2vs 2024+1
020262026 to dateRecords0
Latest Records
Newest first across sources; each opens the record
Dornier Medtech America, Inc.Dornier Medtech AmericaDornier Medtech America Inc (Dmta)
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
