510(k) · Cleared
ClearedSanarus Visica Treatment System
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly
Sanarus Medical, Inc. · GEH Unit, Cryosurgical, Accessories
Cleared on Jul 18, 2006 as substantially equivalent to K022314 (Sanarus Medical, Inc., 2002) and 1 other predicate after a 47-day review. Its family tree reaches back 5 generations to 2001. 27 later devices descend from it.
- Decided
- Jul 18, 2006
- Review
- 47 days
- Class
- Class II
- Product code
- GEH
- Recalls
- None
- Predicates
- 2
Its longest line of descent runs back 5 generations to K003811 (2001). 9 ancestors in all, the oldest K790187 (1979). 27 later devices descend from it, 1 citing it directly.
- Root · 5 generations backK003811 Cryocare Surgical SystemEndocare, Inc. · 2001
- 4 generations backK020605 Sanarus Visica Treatment SystemSanarus Medical, Inc. · 2002
- 3 generations backK021211 Modification to Sanarus Visica Treatment SystemSanarus Medical, Inc. · 2002
- 2 generations backK022314 Sanarus Visica Treatment SystemSanarus Medical, Inc. · 2002 · Recalled
- 1 generation backK052861 Modification to:Sanarus Visica Treatment System , Models VS2000Sanarus Medical, Inc. · 2005
- This deviceK061510 Sanarus Visica Treatment SystemSanarus Medical, Inc. · 2006
- Descendant · cites it directly · 26 of its ownK062896 V2 Treatment System (V2 Console, V2 Ice Probe, V2 Dewars) Models…Sanarus Medical, Inc. · 2007
- Descendant · 2 generations on · 25 of its ownK102360 Icesence 3IceCure Medical, Ltd. · 2010 · Recalled
- Descendant · 3 generations on · 20 of its ownK133258 Trufreeze SystemCSA Medical, Inc. · 2014 · Recalled
- Descendant · 4 generations on · 19 of its ownK143625 truFreeze SystemCSA Medical, Inc. · 2015 · Recalled
- Descendant · 5 generations on · 11 of its ownK150920 truFreeze SystemCSA Medical, Inc. · 2015
Showing 5 of 27 descendants. See all descendants
Descendants cleared per year
Most influential descendants
Showing 5 of 27 · See all- K062896V2 Treatment System (V2 Console, V2 Ice Probe, V2 Dewars) Models; VS3000, VP0600, VD0600Sanarus Medical, Inc. · 2007 · cites it directly26descendants
- K102360Icesence 3IceCure Medical, Ltd. · 2010 · 2 generations on25descendants
- K133258Trufreeze SystemCSA Medical, Inc. · 2014 · 3 generations on20descendants
- K143625truFreeze SystemCSA Medical, Inc. · 2015 · 4 generations on19descendants
- K150920truFreeze SystemCSA Medical, Inc. · 2015 · 5 generations on11descendants
View FIG. 1 as a table
Line of descent and top descendants
| Generation | Number | Device | Applicant | Decided | Recalls |
|---|---|---|---|---|---|
| −5 | K003811 | Cryocare Surgical System | Endocare, Inc. | 2001 | — |
| −4 | K020605 | Sanarus Visica Treatment System | Sanarus Medical, Inc. | 2002 | — |
| −3 | K021211 | Modification to Sanarus Visica Treatment System | Sanarus Medical, Inc. | 2002 | — |
| −2 | K022314 | Sanarus Visica Treatment System | Sanarus Medical, Inc. | 2002 | 1 |
| −1 | K052861 | Modification to:Sanarus Visica Treatment System , Models VS2000 | Sanarus Medical, Inc. | 2005 | — |
| 0 (this device) | K061510 | Sanarus Visica Treatment System | Sanarus Medical, Inc. | 2006 | — |
| +1 | K062896 | V2 Treatment System (V2 Console, V2 Ice Probe, V2 Dewars) Models; VS3000… | Sanarus Medical, Inc. | 2007 | — |
| +2 | K102360 | Icesence 3 | IceCure Medical, Ltd. | 2010 | 1 |
| +3 | K133258 | Trufreeze System | CSA Medical, Inc. | 2014 | 1 |
| +4 | K143625 | truFreeze System | CSA Medical, Inc. | 2015 | 1 |
| +5 | K150920 | truFreeze System | CSA Medical, Inc. | 2015 | — |
Other ancestors by year cleared
| Year cleared | Devices | With a Class I recall |
|---|---|---|
| 1979 | 1 | 0 |
| 1990 | 1 | 0 |
| 1997 | 1 | 0 |
| 2001 | 1 | 0 |
Descendants by year cleared
| Year cleared | Devices | With a Class I recall |
|---|---|---|
| 2007 | 1 | 0 |
| 2010 | 1 | 0 |
| 2014 | 1 | 0 |
| 2015 | 3 | 0 |
| 2016 | 4 | 0 |
| 2017 | 5 | 0 |
| 2018 | 1 | 0 |
| 2019 | 2 | 0 |
| 2020 | 2 | 0 |
| 2021 | 1 | 0 |
| 2022 | 2 | 0 |
| 2024 | 2 | 0 |
| 2025 | 1 | 0 |
| 2026 | 1 | 0 |
Sources: FDA 510(k) database (decision fields), the FDA summary (predicates and indications), FDA recall and enforcement reports, and MAUDE; processed by 510(k) Report. Verify on FDA.gov · Methodology and accuracy.
Planning a device in GEH? A 510(k) Report weighs predicate choices, recall history and review times for a new device like this one.
Top candidate predicates for a new GEH device
- #1 K211099 Freeze’n Clear Skin Clinic Warts & Tagsscore 25.4 · 4 generations · no Class I recall
- #2 Held for the reportin the report
- #3 Held for the reportin the report
What was it cleared against? (2)
Devices the submitter claimed this one is substantially equivalent to (*), and reference devices cited for a specific test or feature (†), as written in the FDA summary.
| Type | Number | Device | Decided |
|---|---|---|---|
| * | K022314 | Sanarus Visica Treatment SystemSummary page 2…s Visica Treatment System is substantially equivalent to the Sanarus Visica Treatment System that was determined to be substantially equivalent on Oct 15 2002 (reference K022314) and on Nov 15 2005 (reference K052861). The Sanarus Visica Treatment System has the same indications for use and technological c… | 2002 |
| * | K052861 | Modification to:Sanarus Visica Treatment System , Models VS2000Summary page 2…lly equivalent to the Sanarus Visica Treatment System that was determined to be substantially equivalent on Oct 15 2002 (reference K022314) and on Nov 15 2005 (reference K052861). The Sanarus Visica Treatment System has the same indications for use and technological characteristics as the predicate device.… | 2005 |
What descends from it? (27)
See all 271 later device cites it directly; ranked here by how many devices descend from each in turn.
| Number | Device | Decided | Descendants |
|---|---|---|---|
| K062896 | V2 Treatment System (V2 Console, V2 Ice Probe, V2 Dewars) Models; VS3000, VP0600, VD0600 | 2007 | 26 |
Has anything in its family been recalled? (0 Class I)
No FDA recall names this device.
No ancestor or descendant has a Class I recall.
What does this lineage say?
- The line of descent spans 5 years and passes through 2 companies; a new generation was cleared every 5 months on median.
- 1 of the 9 ancestors has a recall of any class.
- Of its descendants, K062896 (Sanarus Medical, Inc., 2007) has gone furthest, with 26 descendants of its own.
- 1 other device also cites its predicate K022314.
How does its category compare?
All GEH devicesGEH Unit, Cryosurgical, Accessories: FDA decisions, review times, recalls and adverse event reports over 20 years.
FDA decisions per year · GEH
10in 2025
2026 to Oct 25, outlined.
Median 510(k) review, days · GEH
77in 2025
Receipt to decision; years with fewer than 3 clearances left blank.
Recalls per year · GEH
2in 2023
Class I (0 since 2007) Class II/III not classified
Adverse event reports per year · GEH
171in 2025
MAUDE reports naming product code GEH, not matched to any one device; reports are not rates.
View these four charts as a table
| Year | Decisions | Median 510(k) review, days | Recalls (Class I) | MAUDE reports |
|---|---|---|---|---|
| 2007 | 6 | 71 | 3 | 23 |
| 2008 | 1 | — | 2 | 29 |
| 2009 | 4 | 121 | 13 | 21 |
| 2010 | 4 | 86 | 4 | 173 |
| 2011 | 7 | 91 | 0 | 61 |
| 2012 | 4 | 96 | 3 | 91 |
| 2013 | 4 | 76 | 0 | 91 |
| 2014 | 6 | 42 | 2 | 57 |
| 2015 | 11 | 72 | 0 | 97 |
| 2016 | 15 | 60 | 0 | 143 |
| 2017 | 12 | 83 | 0 | 216 |
| 2018 | 6 | 42 | 1 | 208 |
| 2019 | 6 | 115 | 1 | 455 |
| 2020 | 8 | 113 | 37 | 277 |
| 2021 | 6 | 206 | 0 | 213 |
| 2022 | 6 | 56 | 0 | 230 |
| 2023 | 8 | 136 | 2 | 164 |
| 2024 | 9 | 85 | 0 | 141 |
| 2025 | 10 | 77 | 0 | 171 |
| 2026 | 8 | 148 | 2 | — |
What is it indicated for?
The device is indicated for use in general surgery, gynecology and oncology. The system is designed to destroy tissue by the application of extreme cold temperatures. In addition the system is intended for use in the following indications:
General Surgery
Ablation of breast fibroadenoma
Localization of breast lesions
Gynecology
Ablation of malignant neoplasia or benign dysplasia of the female genitalia
Oncology
Ablation of cancerous or malignant tissue
Ablation of benign tumors
Palliative intervention
Indications for use as stated in the FDA summary.
https://510kreport.com/device/K061510 · printed Nov 6, 2026
Cite this page
510(k) Report. “K061510: Sanarus Visica Treatment System.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K061510
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Record history
- FDA decision record loaded May 2, 2026
- Summary read Oct 13, 2026 (extraction version 9eaa42aa01ed)
- Lineage and recalls computed Nov 3, 2026
- Page last updated Nov 3, 2026