510(k) · Cleared
ClearedVerruca-Freeze H Plus
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly
Cryosurgery, Inc. · GEH Unit, Cryosurgical, Accessories
Cleared on Oct 10, 2025 as substantially equivalent to K243454 (Cryosurgery, Inc., 2024) and 1 other predicate after a 29-day review. Its family tree reaches back 4 generations to 1999.
- Decided
- Oct 10, 2025
- Review
- 29 days
- Class
- Class II
- Product code
- GEH
- Recalls
- None
- Predicates
- 2
Its longest line of descent runs back 4 generations to K990877 (1999). 8 ancestors in all, the oldest K881349 (1988). No later device cites it as a predicate yet.
- Root · 4 generations backK990877 Histofreezer DeviceOraSure Technologies, Inc. · 1999
- 3 generations backK161337 CryoDose H or SimilarNuance Medical, LLC · 2016
- 2 generations backK233347 Verruca-Freeze® HCryosurgery, Inc. · 2023
- 1 generation backK243454 Verruca-Freeze HCryosurgery, Inc. · 2024
- This deviceK252903 Verruca-Freeze H PlusCryosurgery, Inc. · 2025
View FIG. 1 as a table
Line of descent and top descendants
| Generation | Number | Device | Applicant | Decided | Recalls |
|---|---|---|---|---|---|
| −4 | K990877 | Histofreezer Device | OraSure Technologies, Inc. | 1999 | — |
| −3 | K161337 | CryoDose H or Similar | Nuance Medical, LLC | 2016 | — |
| −2 | K233347 | Verruca-Freeze® H | Cryosurgery, Inc. | 2023 | — |
| −1 | K243454 | Verruca-Freeze H | Cryosurgery, Inc. | 2024 | — |
| 0 (this device) | K252903 | Verruca-Freeze H Plus | Cryosurgery, Inc. | 2025 | — |
Other ancestors by year cleared
| Year cleared | Devices | With a Class I recall |
|---|---|---|
| 1988 | 1 | 0 |
| 1994 | 1 | 0 |
| 1999 | 1 | 0 |
| 2013 | 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 |
|---|---|---|---|
| * | K243454 | Verruca-Freeze HSummary page 5…GEH Class 2 5. Primary Predicate Device Device Name Verruca-Freeze® H 510(k) Number K243454 Regulation Number 878.4350 - Cryosurgical unit and accessories Product Code GEH Class… | 2024 |
| * | K130995 | Nuance Cryo-Freeze Spray or Cryo-in-a-Can or Vandolay Freeze SpraySummary page 5…GEH Class 2 6. Predicate Device Device Name Nuance Freeze Spray System 510(k) Number K130995 Regulation Number 878.4350 - Cryosurgical unit and accessories Product Code GEH Class… | 2013 |
| † | K233347 | Verruca-Freeze® H | 2023 |
What descends from it?
No later submission names this one as a predicate yet.
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 26 years and passes through 3 companies; a new generation was cleared every 7.4 years on median.
- None of the 8 ancestors has a recall.
How does its category compare?
All GEH devicesGEH 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
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 Verruca-Freeze H Plus cryosurgical system is intended for use by trained medical professionals to treat the following benign skin lesions:
- Actinic Keratosis
- Genital Warts
- Lentigo
- Molluscum Contagiosum
- Seborrheic Keratosis
- Skin Tags
- Verruca Plantaris
- Verruca Vulgaris
- Verruca Plana
Indications for use as stated in the FDA summary.
https://510kreport.com/device/K252903 · printed Nov 4, 2026
Cite this page
510(k) Report. “K252903: Verruca-Freeze H Plus.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 4, 2026. https://510kreport.com/device/K252903
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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