510(k) Report

510(k) · Cleared

Cleared

Skin Clinic Nitro Clear Wart Remover

K242932510(k) TraditionalCleared Apr 15, 2025202-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

Cryoconcepts LP · GEH Unit, Cryosurgical, Accessories

Cleared on Apr 15, 2025 as substantially equivalent to K211099 (Cryoconcepts LP, 2022) and 1 other predicate after a 202-day review. Its family tree reaches back 6 generations to 1991. 1 later device descends from it.

Decided
Apr 15, 2025
Review
202 days
Class
Class II
Product code
GEH
Recalls
None
Predicates
2

Its longest line of descent runs back 6 generations to K911420 (1991). 19 ancestors in all, the oldest K881349 (1988). 1 later device descends from it, 1 citing it directly.

Other ancestors, by year clearedDescendants, by year cleared 2022: 1 other ancestor2019: 1 other ancestor2003: 2 other ancestors1993: 2 other ancestors2016: 1 other ancestor2002: 1 other ancestor1997: 1 other ancestor2013: 1 other ancestor1999: 1 other ancestor1994: 1 other ancestor1988: 1 other ancestor2025: 1 descendant clearedK911420 · Histofreezer · Solarcare Technologies Corp,Inc. · 1991K023487 · Histofreezer Wart Removal System or Other Proprietary Name · OraSure Technologies, Inc. · 2003 · recalledK101049 · Wart Freeze · Koninklijke Utermohlen NV · 2011K130599 · Wart Freeze · Koninklijke Utermohlen NV · 2013K140314 · Wartie Wart Remover · Yonmedical BV · 2014K172373 · Compound W Nitro-Freeze · Medtech Products, Inc. · 20171990200020102020
Other ancestors, by generationDescendants, by generation 1 generation back: 1 other ancestor2 generations back: 3 other ancestors3 generations back: 5 other ancestors4 generations back: 1 other ancestor5 generations back: 3 other ancestors 1 generation forward: 1 descendant K172373 · Compound W Nitro-Freeze · Medtech Products, Inc. · 2017K140314 · Wartie Wart Remover · Yonmedical BV · 2014K130599 · Wart Freeze · Koninklijke Utermohlen NV · 2013K101049 · Wart Freeze · Koninklijke Utermohlen NV · 2011K023487 · Histofreezer Wart Removal System or Other Proprietary Name · OraSure Technologies, Inc. · 2003 · recalledK911420 · Histofreezer · Solarcare Technologies Corp,Inc. · 1991−50
  1. Root · 6 generations backK911420 HistofreezerSolarcare Technologies Corp,Inc. · 1991
  2. 5 generations backK023487 Histofreezer Wart Removal System or Other Proprietary NameOraSure Technologies, Inc. · 2003 · Recalled
  3. 4 generations backK101049 Wart FreezeKoninklijke Utermohlen NV · 2011
  4. 3 generations backK130599 Wart FreezeKoninklijke Utermohlen NV · 2013
  5. 2 generations backK140314 Wartie Wart RemoverYonmedical BV · 2014
  6. 1 generation backK172373 Compound W Nitro-FreezeMedtech Products, Inc. · 2017
  7. This deviceK242932 Skin Clinic Nitro Clear Wart RemoverCryoconcepts LP · 2025
  8. Descendant · cites it directly · 0 of its ownK253000 CryoFreeze Wart and Skin Tag RemoverCryosurgery, Inc. · 2025

Most influential descendants

Showing 1 of 1 · See all
  • K253000CryoFreeze Wart and Skin Tag RemoverCryosurgery, Inc. · 2025 · cites it directly0descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−6K911420HistofreezerSolarcare Technologies Corp,Inc.1991—
−5K023487Histofreezer Wart Removal System or Other Proprietary NameOraSure Technologies, Inc.20033
−4K101049Wart FreezeKoninklijke Utermohlen NV2011—
−3K130599Wart FreezeKoninklijke Utermohlen NV2013—
−2K140314Wartie Wart RemoverYonmedical BV2014—
−1K172373Compound W Nitro-FreezeMedtech Products, Inc.2017—
0 (this device)K242932Skin Clinic Nitro Clear Wart RemoverCryoconcepts LP2025—
+1K253000CryoFreeze Wart and Skin Tag RemoverCryosurgery, Inc.2025—

Other ancestors by year cleared

Year clearedDevicesWith a Class I recall
198810
199320
199410
199710
199910
200210
200320
201310
201610
201910
202210

Descendants by year cleared

Year clearedDevicesWith a Class I recall
202510
FIG. 1 — Lineage of K242932, 1991–2025Source: 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? (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
*K211099Freeze’n Clear Skin Clinic Warts & Tags
Summary page 5
…ry Regulatory Class: II Code of Federal Regulation: 878.4350 Product Code: GEH III. PREDICATE DEVICES – Class II Skin Clinic Freeze n’ Clear for Skin Tags & Warts K211099 Compound W Nitro-Freeze Wart Remover K172373 IV. DEVICE DESCRIPTION The Skin Clinic Nitro Clear Wart Remover device utilizes…
Cryoconcepts LP2022—
*K172373Compound W Nitro-Freeze
Summary page 5
…lation: 878.4350 Product Code: GEH III. PREDICATE DEVICES – Class II Skin Clinic Freeze n’ Clear for Skin Tags & Warts K211099 Compound W Nitro-Freeze Wart Remover K172373 IV. DEVICE DESCRIPTION The Skin Clinic Nitro Clear Wart Remover device utilizes extreme cold to facilitate the removal of com…
Medtech Products, Inc.2017—

Also cleared against K211099: 6 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
K253000CryoFreeze Wart and Skin Tag RemoverCryosurgery, Inc.20250

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 34 years and passes through 6 companies; a new generation was cleared every 7.4 years on median.
  • 1 of the 19 ancestors has a recall of any class.
  • Of its descendants, K253000 (Cryosurgery, Inc., 2025) has gone furthest, with 0 descendants of its own.
  • 6 other devices also cite its predicate K211099.

How does its category compare?

All GEH devices

GEH Unit, Cryosurgical, Accessories: FDA decisions, review times, recalls and adverse event reports over 20 years. 2025, 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 Skin Clinic Nitro Clear Wart Remover is intended for the OTC treatment of common warts and plantar warts in adults and children 4 years of age and older.

Indications for use as stated in the FDA summary.

Cite this page

510(k) Report. “K242932: Skin Clinic Nitro Clear Wart Remover.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K242932

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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