510(k) Report

510(k) · Cleared

Recalled · Class II · 2020

IcePearl 2.1 CX L, IceForce 2.1 CX L

K162599510(k) SpecialCleared Oct 11, 201622-day reviewClass II21 CFR 878.4350Recalls 2

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

Galil Medical, Ltd. · GEH Unit, Cryosurgical, Accessories

Cleared on Oct 11, 2016 as substantially equivalent to K152133 (Galil Medical, Ltd., 2015) after a 22-day review. Its family tree reaches back 9 generations to 2001. 1 later device descends from it. It has been recalled 2 times.

Decided
Oct 11, 2016
Review
22 days
Class
Class II
Product code
GEH
Recalls
2
Predicates
1

Its longest line of descent runs back 9 generations to K010991 (2001). 22 ancestors in all, the oldest K942299 (1995). 1 later device descends from it, 1 citing it directly.

  1. Root · 9 generations backK010991 Seednet, Models FP6T5, FP5T5, FP5T3Galil Medical, Ltd. · 2001 · Recalled
  2. 5 generations between
  3. 3 generations backK121251 Icerod CX Cryoablation Needle Icerod CX Cryoablation Needle MultipackGalil Medical, Ltd. · 2012 · Recalled
  4. 2 generations backK140584 Icerod CX Cryoablation NeedleGalil Medical, Ltd. · 2014
  5. 1 generation backK152133 IcePearl 2.1 CX Cryoablation Needle, IcePearl 2.1 CX Prostate…Galil Medical, Ltd. · 2015 · Recalled
  6. This deviceK162599 IcePearl 2.1 CX L, IceForce 2.1 CX LGalil Medical, Ltd. · 2016
  7. Descendant · cites it directly · 0 of its ownK203032 IcePearl 2.1 CX 90° Needle, IcePearl 2.1 CX L 90° Needle, IcePearl…Galil Medical, Inc. · 2020
Show all 9 generations
  1. Root · 9 generations backK010991 Seednet, Models FP6T5, FP5T5, FP5T3Galil Medical, Ltd. · 2001 · Recalled
  2. 8 generations backK011950 Seednet, Model FP6T5, FP5T5, FP5T3Galil Medical, Ltd. · 2002
  3. 7 generations backK021261 Seednet System and Seednetgold System, Models GP6T5, GP5T5, GP5T3…Galil Medical, Ltd. · 2002 · Recalled
  4. 6 generations backK031117 Seednet System and Seednetgold SystemGalil Medical, Ltd. · 2003
  5. 5 generations backK042667 Seednet Gold with Renal Kit, Model Fprpr 3021, (Renal Kit), Fprch…Galil Medical, Ltd. · 2004
  6. 4 generations backK060390 Seednet, Seednet Gold, Cryohit, Cryo TheraGalil Medical, Ltd. · 2006 · Recalled
  7. 3 generations backK121251 Icerod CX Cryoablation Needle Icerod CX Cryoablation Needle MultipackGalil Medical, Ltd. · 2012 · Recalled
  8. 2 generations backK140584 Icerod CX Cryoablation NeedleGalil Medical, Ltd. · 2014
  9. 1 generation backK152133 IcePearl 2.1 CX Cryoablation Needle, IcePearl 2.1 CX Prostate…Galil Medical, Ltd. · 2015 · Recalled
  10. This deviceK162599 IcePearl 2.1 CX L, IceForce 2.1 CX LGalil Medical, Ltd. · 2016

Most influential descendants

Showing 1 of 1 · See all
  • K203032IcePearl 2.1 CX 90° Needle, IcePearl 2.1 CX L 90° Needle, IcePearl 2.1 CX Needle…Galil Medical, Inc. · 2020 · cites it directly0descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−9K010991Seednet, Models FP6T5, FP5T5, FP5T3Galil Medical, Ltd.20012
−8K011950Seednet, Model FP6T5, FP5T5, FP5T3Galil Medical, Ltd.2002—
−7K021261Seednet System and Seednetgold System, Models GP6T5, GP5T5, GP5T3, HP5T5 & HP5T3Galil Medical, Ltd.20021
−6K031117Seednet System and Seednetgold SystemGalil Medical, Ltd.2003—
−5K042667Seednet Gold with Renal Kit, Model Fprpr 3021, (Renal Kit), Fprch 2024…Galil Medical, Ltd.2004—
−4K060390Seednet, Seednet Gold, Cryohit, Cryo TheraGalil Medical, Ltd.20068
−3K121251Icerod CX Cryoablation Needle Icerod CX Cryoablation Needle MultipackGalil Medical, Ltd.20121
−2K140584Icerod CX Cryoablation NeedleGalil Medical, Ltd.2014—
−1K152133IcePearl 2.1 CX Cryoablation Needle, IcePearl 2.1 CX Prostate Cryoablation Kit…Galil Medical, Ltd.201518
0 (this device)K162599IcePearl 2.1 CX L, IceForce 2.1 CX LGalil Medical, Ltd.2016—
+1K203032IcePearl 2.1 CX 90° Needle, IcePearl 2.1 CX L 90° Needle, IcePearl 2.1 CX…Galil Medical, Inc.2020—

Other ancestors by year cleared

Year clearedDevicesWith a Class I recall
199510
199610
199810
199920
200020
200110
200520
200610
201120

Descendants by year cleared

Year clearedDevicesWith a Class I recall
202010
FIG. 1 — Lineage of K162599, 2001–2020Source: 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
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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
*K152133IcePearl 2.1 CX Cryoablation Needle, IcePearl 2.1 CX Prostate Cryoablation Kit…
Summary page 4
…21 CFR 878.4350 Predicate Devices / Reference IcePearl 2.1 CX and IceFORCE 2.1 CX Cryoablation 510(k): Needles (K152133) Date of Preparation: September 15, 2016 Device Description: Galil Medical’s IcePearl 2.1 CX L and IceFORCE 2…
Galil Medical, Ltd.201518

Also cleared against K152133: 3 other devices →

What descends from it? (1)

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

NumberDeviceApplicantDecidedDescendants
K203032IcePearl 2.1 CX 90° Needle, IcePearl 2.1 CX L 90° Needle, IcePearl 2.1 CX Needle…Galil Medical, Inc.20200

Has anything in its family been recalled? (0 Class I)

Recalls of this device

DateClassRecallRoot causeReason
Nov 18, 2020Class IIZ-0659-2021Under Investigation by firmComplaint trend regarding needle shaft gas leaks.
Nov 18, 2020Class IIZ-0662-2021Under Investigation by firmComplaint trend regarding needle shaft gas leaks.

No ancestor or descendant has a Class I recall.

What does this lineage say?

  • The line of descent spans 15 years and passes through 1 company; a new generation was cleared every 1.4 years on median.
  • 11 of the 22 ancestors have a recall of any class.
  • Of its descendants, K203032 (Galil Medical, Inc., 2020) has gone furthest, with 0 descendants of its own.
  • 3 other devices also cite its predicate K152133.

How does its category compare?

All GEH devices

GEH Unit, Cryosurgical, Accessories: FDA decisions, review times, recalls and adverse event reports over 20 years. 2016, 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?

Galil Medical’s IcePearl 2.1 CX L and IceFORCE 2.1 CX L Cryoablation Needles are intended for cryoablative destruction of tissue during surgical procedures. The IcePearl 2.1 CX L and IceFORCE 2.1 CX L Cryoablation Needles are indicated for use as a cryosurgical tool in the fields of general surgery, dermatology, neurology (including cryoanalgesia), thoracic surgery (with the exception of cardiac tissue), ENT, gynecology, oncology, proctology, and…

Read the full statement (274 words)

Galil Medical’s IcePearl 2.1 CX L and IceFORCE 2.1 CX L Cryoablation Needles are intended for cryoablative destruction of tissue during surgical procedures. The IcePearl 2.1 CX L and IceFORCE 2.1 CX L Cryoablation Needles are indicated for use as a cryosurgical tool in the fields of general surgery, dermatology, neurology (including cryoanalgesia), thoracic surgery (with the exception of cardiac tissue), ENT, gynecology, oncology, proctology, and urology. The systems are designed to destroy tissue by the application of extreme cold temperatures including prostate and kidney tissue, liver metastases, tumors, skin lesions, and warts.

The Galil Medical IcePearl 2.1 CX L and IceFORCE 2.1 CX L Cryoablation Needles have the following specific indications:

• Urology (ablation of prostate tissue in cases of prostate cancer and Benign Prostate Hyperplasia "BPH")

• Oncology (ablation of cancerous or malignant tissue and benign tumors, and palliative intervention)

• Dermatology (ablation or freezing of skin cancers and other cutaneous disorders. Destruction of warts or lesions, angiomas, sebaceous hyperplasia, basal cell tumors of the eyelid or canthus area, ulcerated basal cell tumors, dermatofibromas small hemanglomas, mucocele cysts, multiple warts, plantar warts, actinic and seborrheic keratoses, cavernous hemanglomas, perianal condylomata, and palliation of tumors of the skin.)

• Gynecology (ablation of malignant neoplasia or benign dysplasia of the female genitalia)

• General surgery (palliation of tumors of the rectum, hemorrhoids, anal fissures, pilonidal cysts, and recurrent cancerous lesions, ablation of breast fibroadenoma)

• ENT (Palliation of tumors of the oral cavity and ablation of leukoplakia of the mouth)

• Thoracic surgery (with the exception of cardiac tissue)

• Proctology (ablation of benign or malignant growths of the anus or rectum, and hemorrhoids)

Indications for use as stated in the FDA summary.

Cite this page

510(k) Report. “K162599: IcePearl 2.1 CX L, IceForce 2.1 CX L.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K162599

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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