Hydrocision, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Hydrocision, Inc. - FDA 510(k) Cleared Devices
Recent clearances: SpineSite Endoscope System, HydroCision SpineJet System, HydroCision TenJet Device
12
Total
12
Cleared
0
Denied
Hydrocision, Inc. has 12 FDA 510(k) cleared medical devices. Based in Hopkonton, US.
Latest FDA clearance: Jul 2025. Active since 1998. Primary specialty: Orthopedic.
Browse the FDA 510(k) cleared devices submitted by Hydrocision, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Mae Consulting Group, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - Hydrocision, Inc.
12 devices
Cleared
Jul 30, 2025
SpineSite Endoscope System
Orthopedic
387d
Cleared
Apr 16, 2020
HydroCision SpineJet System
Orthopedic
27d
Cleared
Jun 05, 2019
HydroCision TenJet Device
General & Plastic Surgery
68d
Cleared
Jul 28, 2004
ARTHROJET XT
Orthopedic
79d
Cleared
Sep 16, 2003
HYDROCISION ARTHROJET SYSTEM WITH CAUTERY, TURBOBURR AND CURETTE, MODELS...
Orthopedic
32d
Cleared
May 09, 2003
HYDROCISION GENERAL SURGERY FLUIDJET SYSTEM
General Hospital
340d
Cleared
Apr 03, 2002
HYDROCISION ARTHOJET SYSTEM WITH CAUTERY AND TURBOBURR
Orthopedic
30d
Cleared
Jun 22, 2001
MODIFICATION TO HYDROCISION DEBRIDEMENT SYSTEM
General Hospital
28d
Cleared
Nov 24, 2000
HYDROCISION ARTHROJET SYSTEM WITH CAUTERY AND BURR
Orthopedic
80d
Cleared
Mar 31, 2000
HYDROCISION DEBDRIDEMENT SYSTEM
General Hospital
345d
Cleared
Oct 25, 1999
HYDROCISION ARTHROJET SYSTEM WITH CAUTERY
Orthopedic
48d
Cleared
Sep 25, 1998
HYDROCISION ARTHROJET SYSTEM
Orthopedic
88d