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Hydrocision, Inc.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
12
Inspections
4
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K241990SpineSite Endoscope SystemJuly 30, 2025
K200729HydroCision SpineJet SystemApril 16, 2020
K190804HydroCision TenJet DeviceJune 5, 2019
K041233ARTHROJET XTJuly 28, 2004
K032529HYDROCISION ARTHROJET SYSTEM WITH CAUTERY, TURBOBURR AND CURETTE, MODELS 51300, 51310September 16, 2003
K021813HYDROCISION GENERAL SURGERY FLUIDJET SYSTEMMay 9, 2003
K020688HYDROCISION ARTHOJET SYSTEM WITH CAUTERY AND TURBOBURRApril 3, 2002
K011612MODIFICATION TO HYDROCISION DEBRIDEMENT SYSTEMJune 22, 2001
K002764HYDROCISION ARTHROJET SYSTEM WITH CAUTERY AND BURRNovember 24, 2000
K991383HYDROCISION DEBDRIDEMENT SYSTEMMarch 31, 2000
K993009HYDROCISION ARTHROJET SYSTEM WITH CAUTERYOctober 25, 1999
K982266HYDROCISION ARTHROJET SYSTEMSeptember 25, 1998