Hydrocision, Inc.
12 FDA 510(k) clearances · Manufacturer
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| Record | Firm | Date |
|---|---|---|
| SpineSite Endoscope System (K241990) | Hydrocision, Inc. | 2025-07-30 |
| HydroCision SpineJet System (K200729) | Hydrocision, Inc. | 2020-04-16 |
| HydroCision TenJet Device (K190804) | Hydrocision, Inc. | 2019-06-05 |
| ARTHROJET XT (K041233) | Hydrocision, Inc. | 2004-07-28 |
| HYDROCISION ARTHROJET SYSTEM WITH CAUTERY, TURBOBURR AND CURETTE, MODELS 51300, 51310 (K032529) | Hydrocision, Inc. | 2003-09-16 |
| HYDROCISION GENERAL SURGERY FLUIDJET SYSTEM (K021813) | Hydrocision, Inc. | 2003-05-09 |
| HYDROCISION ARTHOJET SYSTEM WITH CAUTERY AND TURBOBURR (K020688) | Hydrocision, Inc. | 2002-04-03 |
| MODIFICATION TO HYDROCISION DEBRIDEMENT SYSTEM (K011612) | Hydrocision, Inc. | 2001-06-22 |
| HYDROCISION ARTHROJET SYSTEM WITH CAUTERY AND BURR (K002764) | Hydrocision, Inc. | 2000-11-24 |
| HYDROCISION DEBDRIDEMENT SYSTEM (K991383) | Hydrocision, Inc. | 2000-03-31 |
| HYDROCISION ARTHROJET SYSTEM WITH CAUTERY (K993009) | Hydrocision, Inc. | 1999-10-25 |
| HYDROCISION ARTHROJET SYSTEM (K982266) | Hydrocision, Inc. | 1998-09-25 |
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Every clearance here is in the API, with alerts when new ones post.