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 13, 2026, FDA's public records list Hydrocision with 12 510(k) clearances. The most recent is a 510(k) clearance dated Jul 30, 2025: SpineSite Endoscope 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.
| Date | Record | Source |
|---|---|---|
| Jul 30, 2025 | SpineSite Endoscope SystemK241990 · HRX | 510(k) clearances |
| Apr 16, 2020 | HydroCision SpineJet SystemK200729 · HRX | 510(k) clearances |
| Jun 5, 2019 | HydroCision TenJet DeviceK190804 · HRX | 510(k) clearances |
| Jul 28, 2004 | ARTHROJET XTK041233 · HRX | 510(k) clearances |
| Sep 16, 2003 | HYDROCISION ARTHROJET SYSTEM WITH CAUTERY, TURBOBURR AND CURETTE, MODELS 51300, 51310K032529 · HRX | 510(k) clearances |
| May 9, 2003 | HYDROCISION GENERAL SURGERY FLUIDJET SYSTEMK021813 · FQH | 510(k) clearances |
| Apr 3, 2002 | HYDROCISION ARTHOJET SYSTEM WITH CAUTERY AND TURBOBURRK020688 · HRX | 510(k) clearances |
| Jun 22, 2001 | MODIFICATION TO HYDROCISION DEBRIDEMENT SYSTEMK011612 · FQH | 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
