Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field.. FDA files no records under this name; these are its 4 companies' records, each linked to the record.
As of Nov 13, 2026, FDA's public records list Nordson and its 4 subsidiaries with 91 510(k) clearances and 9 device recalls. The most recent is a 510(k) clearance dated Dec 18, 2024: Lyka® PORT Needle Free Access Device (4170Y).
Drug approvals, 510(k) clearances, recalls and letters, 2017 to 2026 to date, Nordson and its 4 subsidiaries
A hatched bar is a year that is not over, so its count covers only part of the year.
| Dec 18, 2024 | Lyka® PORT Needle Free Access Device (4170Y)K241058 · FPA | 510(k) clearances |
| Jul 15, 2024 | Endoscopic Applicator, 41 cmK241739 · GCJ | 510(k) clearances |
| Jun 5, 2022 | Q2 Blood Administration SetsK213846 · FPA | 510(k) clearances |
| Jun 2, 2022 | Q2 IV Administration SetsK213588 · FPA | 510(k) clearances |
| Jan 21, 2021 | Precision Delivery Infusion SetK202672 · FPA | 510(k) clearances |
| Nov 20, 2020 | MPS 3 ND Myocardial Protection SystemK201984 · DTR | 510(k) clearances |
| Jun 19, 2020 | MPS 3 Myocardial Protection SystemK200438 · DTR | 510(k) clearances |
| Nov 6, 2018 | MiniGuard Arterial Safety ValveK182442 · MJJ | 510(k) clearances |
| Oct 20, 2016 | Nordson Micromedics FibriJet Endoscopic Catheter Introducer, Catalog Number SA-3445. Sterilized using Ethylene OxideClass II · The sterile packaging may contain small channels in the seal of the pouch, If the channels are present, the package int | Device recalls |
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
