510(k) Report

510(k) · Cleared

Cleared

Cryocare CS-3 Surgical System version 5

K151968510(k) TraditionalCleared Sep 9, 201555-day reviewClass II21 CFR 878.4350

Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly, last Nov 3, 2026

Healthtronics · GEH Unit, Cryosurgical, Accessories

Cleared on Sep 9, 2015 as substantially equivalent to K141110 (Healthtronics, 2015) after a 55-day review. Its family tree reaches back 9 generations to 1993. 6 later devices descend from it.

Decided
Sep 9, 2015
Review
55 days
Class
Class II
Product code
GEH
Recalls
None
Predicates
1

Its longest line of descent runs back 9 generations to K926514 (1993). 20 ancestors in all, the oldest K850478 (1985). 6 later devices descend from it, 1 citing it directly.

  1. Root · 9 generations backK926514 Endoscopic Ultrasound System Type 20Olympus Corp. · 1993 · Recalled
  2. 5 generations between
  3. 3 generations backK060279 Cryocare CS Surgical SystemEndocare, Inc. · 2006 · Recalled
  4. 2 generations backK101333 Cryocare CS Surgical SystemEndocare, Inc. · 2010 · Recalled
  5. 1 generation backK141110 Cryocare CS Surgical SystemHealthtronics · 2015
  6. This deviceK151968 Cryocare CS-3 Surgical System version 5Healthtronics · 2015
  7. Descendant · cites it directly · 5 of its ownK153489 Cryocare CS Surgical SystemHealthtronics · 2016
  8. Descendant · 2 generations on · 4 of its ownK201588 CRYOCARE TOUCH System and Accessories, Endocare 1.7mm Round Ice…Varian Medical Systems, Inc. · 2020
  9. Descendant · 3 generations on · 1 of its ownK230271 ISOLIS CryoprobeVarian Medical Systems, Inc. · 2023
  10. Descendant · 3 generations on · 0 of its ownK250742 Focused Cryotherapy SystemFocused Cryo, Inc. · 2025
  11. Descendant · 3 generations on · 0 of its ownK243042 Co-Ablation System with Sterile Co-Ablation ProbeHygea Medical Technology Co., Ltd. · 2025
Show all 9 generations
  1. Root · 9 generations backK926514 Endoscopic Ultrasound System Type 20Olympus Corp. · 1993 · Recalled
  2. 8 generations backK963023 Ultrasound Gastroscope GF Type UM30POlympus America, Inc. · 1997
  3. 7 generations backK994373 Hdi 1500/SA 8800 Ultrasound System with Multiplane Transesophageal…Atl Ultrasound, Inc. · 2000
  4. 6 generations backK030191 Terason Model 2000/Bas Portable Ultrasound SystemTeratech Corp. · 2003
  5. 5 generations backK032333 Cryocare CS Surgical SystemEndocare, Inc. · 2003
  6. 4 generations backK050347 Modification to Cryocare CS Surgical SystemEndocare, Inc. · 2005
  7. 3 generations backK060279 Cryocare CS Surgical SystemEndocare, Inc. · 2006 · Recalled
  8. 2 generations backK101333 Cryocare CS Surgical SystemEndocare, Inc. · 2010 · Recalled
  9. 1 generation backK141110 Cryocare CS Surgical SystemHealthtronics · 2015
  10. This deviceK151968 Cryocare CS-3 Surgical System version 5Healthtronics · 2015

Showing 5 of 6 descendants. See all descendants

Descendants cleared per year

2016: 12020: 12023: 22025: 2
2016high 2 (2023) · low 0 (2017)2026

Most influential descendants

Showing 5 of 6 · See all
  • K153489Cryocare CS Surgical SystemHealthtronics · 2016 · cites it directly5descendants
  • K201588CRYOCARE TOUCH System and Accessories, Endocare 1.7mm Round Ice PerCryo Cryoprobe…Varian Medical Systems, Inc. · 2020 · 2 generations on4descendants
  • K230271ISOLIS CryoprobeVarian Medical Systems, Inc. · 2023 · 3 generations on1descendant
  • K250742Focused Cryotherapy SystemFocused Cryo, Inc. · 2025 · 3 generations on0descendants
  • K243042Co-Ablation System with Sterile Co-Ablation ProbeHygea Medical Technology Co., Ltd. · 2025 · 3 generations on0descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−9K926514Endoscopic Ultrasound System Type 20Olympus Corp.19931
−8K963023Ultrasound Gastroscope GF Type UM30POlympus America, Inc.1997—
−7K994373Hdi 1500/SA 8800 Ultrasound System with Multiplane Transesophageal Ultrasound…Atl Ultrasound, Inc.2000—
−6K030191Terason Model 2000/Bas Portable Ultrasound SystemTeratech Corp.2003—
−5K032333Cryocare CS Surgical SystemEndocare, Inc.2003—
−4K050347Modification to Cryocare CS Surgical SystemEndocare, Inc.2005—
−3K060279Cryocare CS Surgical SystemEndocare, Inc.20063
−2K101333Cryocare CS Surgical SystemEndocare, Inc.20102
−1K141110Cryocare CS Surgical SystemHealthtronics2015—
0 (this device)K151968Cryocare CS-3 Surgical System version 5Healthtronics2015—
+1K153489Cryocare CS Surgical SystemHealthtronics2016—
+2K201588CRYOCARE TOUCH System and Accessories, Endocare 1.7mm Round Ice PerCryo…Varian Medical Systems, Inc.2020—
+3K230271ISOLIS CryoprobeVarian Medical Systems, Inc.2023—
+3K250742Focused Cryotherapy SystemFocused Cryo, Inc.2025—
+3K243042Co-Ablation System with Sterile Co-Ablation ProbeHygea Medical Technology Co., Ltd.2025—

Other ancestors by year cleared

Year clearedDevicesWith a Class I recall
198510
198610
199410
199710
199920
200010
200110
200220
200410

Descendants by year cleared

Year clearedDevicesWith a Class I recall
201610
202010
202320
202520
FIG. 1 — Lineage of K151968, 1993–2025Source: FDA 510(k) summaries, read by 510(k) Report · How lineage is built

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Notable FDA decisions, review times and new Class I recalls. See an issue.

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. #1 K211099 Freeze’n Clear Skin Clinic Warts & Tagsscore 25.4 · 4 generations · no Class I recall
  2. #2 Held for the reportin the report
  3. #3 Held for the reportin the report
Get a 510(k) Report

What was it cleared against? (1)

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.

TypeNumberDeviceApplicantDecidedRecalls
*K141110Cryocare CS Surgical System
Summary page 5
…GEH REGULATION NUMBER: 21 CFR 878.4350 PREDICATE DEVICE: Cryocare CS Surgical System K141110 Cleared 06/25/2015 PRODUCT DESCRIPTION: The Endocare Cryocare CS Surgical System is a mobile console system intended fo…
Healthtronics2015—

Also cleared against K141110: 1 other device →

What descends from it? (6)

1 later device cites it directly; ranked here by how many devices descend from each in turn.

NumberDeviceApplicantDecidedDescendants
K153489Cryocare CS Surgical SystemHealthtronics20165

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 22 years and passes through 6 companies; a new generation was cleared every 2.9 years on median.
  • 6 of the 20 ancestors have a recall of any class.
  • Of its descendants, K153489 (Healthtronics, 2016) has gone furthest, with 5 descendants of its own.
  • 1 other device also cites its predicate K141110.

How does its category compare?

All GEH devices

GEH Unit, Cryosurgical, Accessories: FDA decisions, review times, recalls and adverse event reports over 20 years. 2015, this device’s year, is highlighted.

FDA decisions per year · GEH

10in 2025

2007: 62008: 12009: 42010: 42011: 72012: 42013: 42014: 62015: 112016: 152017: 122018: 62019: 62020: 82021: 62022: 62023: 82024: 92025: 102026 (partial year): 8
2007high 15 (2016) · low 1 (2008)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · GEH

77in 2025

2007: 71 days median2009: 121 days median2010: 86 days median2011: 91 days median2012: 96 days median2013: 76 days median2014: 42 days median2015: 72 days median2016: 60 days median2017: 83 days median2018: 42 days median2019: 115 days median2020: 113 days median2021: 206 days median2022: 56 days median2023: 136 days median2024: 85 days median2025: 77 days median2026 (partial year): 148 days median
2007high 206 (2021) · low 42 (2014)2026

Receipt to decision; years with fewer than 3 clearances left blank.

Recalls per year · GEH

2in 2023

2007: 32008: 22009: 132010: 42012: 32014: 22018: 12019: 12020: 372023: 22026 (partial year): 2
2007high 37 (2020) · low 0 (2011)2026

Class I (0 since 2007) Class II/III not classified

Adverse event reports per year · GEH

171in 2025

2007: 232008: 292009: 212010: 1732011: 612012: 912013: 912014: 572015: 972016: 1432017: 2162018: 2082019: 4552020: 2772021: 2132022: 2302023: 1642024: 1412025: 171
2007high 455 (2019) · low 21 (2009)2025

MAUDE reports naming product code GEH, not matched to any one device; reports are not rates.

View these four charts as a table
YearDecisionsMedian 510(k) review, daysRecalls (Class I)MAUDE reports
2007671323
20081—229
200941211321
20104864173
2011791061
2012496391
2013476091
2014642257
20151172097
201615600143
201712830216
20186421208
201961151455
2020811337277
202162060213
20226560230
202381362164
20249850141
202510770171
202681482—

What is it indicated for?

The Cryocare CS Surgical System is intended for use in open, minimally invasive or endoscopic surgical procedures in the areas in general surgery, urology, gynecology, oncology, neurology, dermatology, ENT, proctology, pulmonary surgery and thoracic surgery. The system is designed to freeze/ablate tissue by the application of extreme cold temperatures including prostate and kidney tissue, liver metastases, tumors, skin lesions, and warts. In addition…

Read the full statement (236 words)

The Cryocare CS Surgical System is intended for use in open, minimally invasive or endoscopic surgical procedures in the areas in general surgery, urology, gynecology, oncology, neurology, dermatology, ENT, proctology, pulmonary surgery and thoracic surgery. The system is designed to freeze/ablate tissue by the application of extreme cold temperatures including prostate and kidney tissue, liver metastases, tumors, skin lesions, and warts.

In addition, the system is intended for use in the following indications:

General Surgery

• Destruction of warts or lesions

• Palliation of tumors of the oral cavity, rectum and skin

• Ablation of leukoplakia of the mouth, angiomas, sebaceous hyperplasia, basal cell tumors of the eyelid or canthus area, ulcerated basal cell tumors, dermatofibromas, small hemangiomas, mucocele cysts, multiple warts, plantar warts, hemorrhoids, anal fissures, perianal condylomata, pilonidal cysts, actinic and seborrheic keratoses, cavernous hemangiomas, recurrent cancerous lesions

Urology

• Ablation of prostate tissue in cases of prostate cancer and benign prostatic hyperplasia

• 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

Neurology

• Freezing of nerve tissue in pain management/cryoanalgesia

Dermatology

• Ablation or freezing of skin cancers and other cutaneous disorders

Proctology

• Ablation of benign or malignant growths of the anus or rectum

• Ablation of hemorrhoids

Thoracic Surgery

• Ablation of arrhythmic cardiac tissue

• Ablation of cancerous lesions

Indications for use as stated in the FDA summary.

Cite this page

510(k) Report. “K151968: Cryocare CS-3 Surgical System version 5.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K151968

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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