510(k) Report

510(k) · Cleared

Cleared

Cryocare CS Surgical System

K141110510(k) TraditionalCleared Jun 25, 2015422-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 Jun 25, 2015 as substantially equivalent to K101333 (Endocare, Inc., 2010) and 1 other predicate after a 422-day review. Its family tree reaches back 8 generations to 1993. 7 later devices descend from it.

Decided
Jun 25, 2015
Review
422 days
Class
Class II
Product code
GEH
Recalls
None
Predicates
2

Its longest line of descent runs back 8 generations to K926514 (1993). 19 ancestors in all, the oldest K850478 (1985). 7 later devices descend from it, 2 citing it directly.

Other ancestors, by year clearedDescendants, by year cleared 2002: 2 other ancestors2004: 1 other ancestor2000: 1 other ancestor2001: 1 other ancestor1999: 2 other ancestors1997: 1 other ancestor1986: 1 other ancestor1985: 1 other ancestor1994: 1 other ancestor2015: 1 descendant cleared2016: 1 descendant cleared2020: 1 descendant cleared2023: 2 descendants cleared2025: 2 descendants clearedK926514 · Endoscopic Ultrasound System Type 20 · Olympus Corp. · 1993 · recalledK963023 · Ultrasound Gastroscope GF Type UM30P · Olympus America, Inc. · 1997K994373 · Hdi 1500/SA 8800 Ultrasound System with Multiplane Transesophageal Ultrasound Transducer (MTP7-4) · Atl Ultrasound, Inc. · 2000K030191 · Terason Model 2000/Bas Portable Ultrasound System · Teratech Corp. · 2003K032333 · Cryocare CS Surgical System · Endocare, Inc. · 2003K050347 · Modification to Cryocare CS Surgical System · Endocare, Inc. · 2005K060279 · Cryocare CS Surgical System · Endocare, Inc. · 2006 · recalledK101333 · Cryocare CS Surgical System · Endocare, Inc. · 2010 · recalled1990200020102020
  1. Root · 8 generations backK926514 Endoscopic Ultrasound System Type 20Olympus Corp. · 1993 · Recalled
  2. 7 generations backK963023 Ultrasound Gastroscope GF Type UM30POlympus America, Inc. · 1997
  3. 6 generations backK994373 Hdi 1500/SA 8800 Ultrasound System with Multiplane Transesophageal…Atl Ultrasound, Inc. · 2000
  4. 5 generations backK030191 Terason Model 2000/Bas Portable Ultrasound SystemTeratech Corp. · 2003
  5. 4 generations backK032333 Cryocare CS Surgical SystemEndocare, Inc. · 2003
  6. 3 generations backK050347 Modification to Cryocare CS Surgical SystemEndocare, Inc. · 2005
  7. 2 generations backK060279 Cryocare CS Surgical SystemEndocare, Inc. · 2006 · Recalled
  8. 1 generation backK101333 Cryocare CS Surgical SystemEndocare, Inc. · 2010 · Recalled
  9. This deviceK141110 Cryocare CS Surgical SystemHealthtronics · 2015
  10. Descendant · cites it directly · 6 of its ownK151968 Cryocare CS-3 Surgical System version 5Healthtronics · 2015
  11. Descendant · cites it directly · 5 of its ownK153489 Cryocare CS Surgical SystemHealthtronics · 2016
  12. Descendant · 2 generations on · 4 of its ownK201588 CRYOCARE TOUCH System and Accessories, Endocare 1.7mm Round Ice…Varian Medical Systems, Inc. · 2020
  13. Descendant · 3 generations on · 1 of its ownK230271 ISOLIS CryoprobeVarian Medical Systems, Inc. · 2023
  14. Descendant · 3 generations on · 0 of its ownK250742 Focused Cryotherapy SystemFocused Cryo, Inc. · 2025

Showing 5 of 7 descendants. See all descendants

Descendants cleared per year

2015: 12016: 12020: 12023: 22025: 2
2015high 2 (2023) · low 0 (2017)2026

Most influential descendants

Showing 5 of 7 · See all
  • K151968Cryocare CS-3 Surgical System version 5Healthtronics · 2015 · cites it directly6descendants
  • 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
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−8K926514Endoscopic Ultrasound System Type 20Olympus Corp.19931
−7K963023Ultrasound Gastroscope GF Type UM30POlympus America, Inc.1997—
−6K994373Hdi 1500/SA 8800 Ultrasound System with Multiplane Transesophageal Ultrasound…Atl Ultrasound, Inc.2000—
−5K030191Terason Model 2000/Bas Portable Ultrasound SystemTeratech Corp.2003—
−4K032333Cryocare CS Surgical SystemEndocare, Inc.2003—
−3K050347Modification to Cryocare CS Surgical SystemEndocare, Inc.2005—
−2K060279Cryocare CS Surgical SystemEndocare, Inc.20063
−1K101333Cryocare CS Surgical SystemEndocare, Inc.20102
0 (this device)K141110Cryocare CS Surgical SystemHealthtronics2015—
+1K151968Cryocare 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—

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
201510
201610
202010
202320
202520
FIG. 1 — Lineage of K141110, 1993–2025Source: FDA 510(k) summaries, read by 510(k) Report · How lineage is built

Get the monthly Device Review Tracker

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? (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.

TypeNumberDeviceApplicantDecidedRecalls
*K101333Cryocare CS Surgical System
Summary page 5
…LASSIFICATION NAME: Cryosurgical Unit and Accessories CLASS: 11 PRODUCT CODE: GEH REGULATION NUMBER: 21 CFR 878.4350 PREDICATE DEVICE: Cryocare CS®-3 Surgical System K101333 Cleared 06/14/2010 Endocare® 2.4mm V-Probe™ Cryoprobe | K101333 Cleared 06/14/2010 Endocare® 2.4 mm Cryoprobe K011074 Cleared 02/…
Endocare, Inc.20102
*K011074Cryocare Surgical System
Summary page 5
…PREDICATE DEVICE: Cryocare CS®-3 Surgical System K101333 Cleared 06/14/2010 Endocare® 2.4mm V-Probe™ Cryoprobe | K101333 Cleared 06/14/2010 Endocare® 2.4 mm Cryoprobe K011074 Cleared 02/28/2006 PRODUCT DESCRIPTION: The Endocare™ Cryocare CS® Surgical System is a mobile console system intended for cryo…
Endocare, Inc.20022

What descends from it? (7)

2 later devices cite it directly; ranked here by how many devices descend from each in turn.

NumberDeviceApplicantDecidedDescendants
K151968Cryocare CS-3 Surgical System version 5Healthtronics20156
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 3.1 years on median.
  • 6 of the 19 ancestors have a recall of any class.
  • Of its descendants, K151968 (Healthtronics, 2015) has gone furthest, with 6 descendants of its own.

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 read by OCR from a scanned FDA summary, so letters may be misread. Check the PDF before quoting it.

Cite this page

510(k) Report. “K141110: Cryocare CS Surgical System.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K141110

Report an extraction error

Tell us what is wrong; we check it against the FDA summary.

Are you the manufacturer?

Send a correction or an update to this page, for example a newer model or a public statement about a recall.

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