Hydrocision, Inc.
Hydrocision, Inc. holds FDA 510(k) medical device clearances, first cleared 1998, most recent 2025.
Top product codes for Hydrocision, Inc.
Recent clearances by Hydrocision, Inc.
- K241990 — SpineSite Endoscope System
- K200729 — HydroCision SpineJet System
- K190804 — HydroCision TenJet Device
- K041233 — ARTHROJET XT
- K032529 — HYDROCISION ARTHROJET SYSTEM WITH CAUTERY, TURBOBURR AND CURETTE, MODELS 51300, 51310
- K021813 — HYDROCISION GENERAL SURGERY FLUIDJET SYSTEM
- K020688 — HYDROCISION ARTHOJET SYSTEM WITH CAUTERY AND TURBOBURR
- K011612 — MODIFICATION TO HYDROCISION DEBRIDEMENT SYSTEM
- K002764 — HYDROCISION ARTHROJET SYSTEM WITH CAUTERY AND BURR
- K991383 — HYDROCISION DEBDRIDEMENT SYSTEM
- K993009 — HYDROCISION ARTHROJET SYSTEM WITH CAUTERY
- K982266 — HYDROCISION ARTHROJET SYSTEM
Data sourced from openFDA. This site is unofficial and independent of the FDA.