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., part of BioventusLabelled 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 14, 2026, FDA's public records list Misonix, Inc. with 19 510(k) clearances. The most recent is a 510(k) clearance dated Jul 30, 2026: neXus Ultrasonic Surgical Aspirator System.
Drug approvals, 510(k) clearances, recalls and letters, 2017 to 2026 to date
A hatched bar is a year that is not over, so its count covers only part of the year.
| Jul 30, 2026 | neXus Ultrasonic Surgical Aspirator SystemK261448 · LFL | 510(k) clearances |
| Jun 23, 2023 | neXus Ultrasonic Surgical Aspirator SystemK231117 · LFL | 510(k) clearances |
| Jul 28, 2022 | neXus Ultrasonic Surgical Aspirator SystemK221235 · LFL | 510(k) clearances |
| Dec 13, 2021 | neXus Ultrasonic Surgical Aspirator SystemK212060 · LFL | 510(k) clearances |
| May 30, 2019 | neXus Ultrasonic Surgical Aspirator SystemK190160 · LFL | 510(k) clearances |
| Mar 5, 2013 | SONICONE PLUS ULTRASOUND WOUND CARE SYSTEM AND ACCESSORIESK123980 · NRB | 510(k) clearances |
| Dec 1, 2011 | MISONIX SONICONE(R) ULTRASONIC WOUND CARE SYSTEM AND ACCESSORIESK112782 · NRB | 510(k) clearances |
| Jul 9, 2008 | SONATHERM 600I ULTRASONIC LESION GENERATING SYSTEMK070779 · NTB | 510(k) clearances |
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
