Hydrocision, Inc.
Hydrocision, Inc. appears in FDA public data with 0 recalls, 12 510(k) clearances, 4 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on Jul 30, 2025.
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 12
- Inspections
- 4
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|---|---|
| K241990 | SpineSite Endoscope System | Jul 30, 2025 |
| K200729 | HydroCision SpineJet System | Apr 16, 2020 |
| K190804 | HydroCision TenJet Device | Jun 5, 2019 |
| K041233 | ARTHROJET XT | Jul 28, 2004 |
| K032529 | HYDROCISION ARTHROJET SYSTEM WITH CAUTERY, TURBOBURR AND CURETTE, MODELS 51300, 51310 | Sep 16, 2003 |
| K021813 | HYDROCISION GENERAL SURGERY FLUIDJET SYSTEM | May 9, 2003 |
| K020688 | HYDROCISION ARTHOJET SYSTEM WITH CAUTERY AND TURBOBURR | Apr 3, 2002 |
| K011612 | MODIFICATION TO HYDROCISION DEBRIDEMENT SYSTEM | Jun 22, 2001 |
| K002764 | HYDROCISION ARTHROJET SYSTEM WITH CAUTERY AND BURR | Nov 24, 2000 |
| K991383 | HYDROCISION DEBDRIDEMENT SYSTEM | Mar 31, 2000 |
| K993009 | HYDROCISION ARTHROJET SYSTEM WITH CAUTERY | Oct 25, 1999 |
| K982266 | HYDROCISION ARTHROJET SYSTEM | Sep 25, 1998 |