Cryosurgery, Inc.: FDA filings under this applicant name
FDA lists 9 510(k) clearances under the applicant name “Cryosurgery, Inc.” (first 1994, latest 2026), across 2 product codes in 2 review panels. Median 510(k) review time under this name: 107 days. Since 2017 the median was 48 days, against 93 days for all cleared 510(k)s in the same product codes. Related companies, subsidiaries and acquired businesses that file under other applicant names are counted on their own pages, not here.
510(k) clearances per year
| Year | Clearances | Median review days |
|---|---|---|
| 2012 | 0 | — |
| 2013 | 0 | — |
| 2014 | 0 | — |
| 2015 | 0 | — |
| 2016 | 0 | — |
| 2017 | 0 | — |
| 2018 | 0 | — |
| 2019 | 0 | — |
| 2020 | 0 | — |
| 2021 | 0 | — |
| 2022 | 0 | — |
| 2023 | 1 | 66 |
| 2024 | 1 | 26 |
| 2025 | 3 | 29 |
| 2026 | 1 | 107 |
Review time against the same product codes
Since 2017, 510(k)s cleared under the name Cryosurgery, Inc. took a median 48 days from FDA receipt to decision. All cleared 510(k)s in the same product codes over the same years took a median 93 days.
Top product codes
| Product code | Device | Submissions | 510(k) clearances |
|---|---|---|---|
| GEH | Unit, Cryosurgical, Accessories | 8 | 8 |
| MLY | Vapocoolant Device | 1 | 1 |
Review panels
Most recent Cryosurgery, Inc. 510(k) clearances
| 510(k) | Device | Product code | Decision date | Review days |
|---|---|---|---|---|
| K261684 | FreezeSpray TA | MLY | 2026-09-05 | 107 |
| K253000 | CryoFreeze Wart and Skin Tag Remover | GEH | 2025-10-16 | 28 |
| K252903 | Verruca-Freeze H Plus | GEH | 2025-10-10 | 29 |
| K243487 | CryoFreeze Wart and Skin Tag Remover | GEH | 2025-03-13 | 125 |
| K243454 | Verruca-Freeze H | GEH | 2024-12-03 | 26 |
| K233347 | Verruca-Freeze® H | GEH | 2023-12-04 | 66 |
| K982506 | VERRUCA-FREEZE CRYOSURGERY DELIVERY SYSTEM | GEH | 1999-01-27 | 191 |
| K955083 | VERRUCA-FREEZE CRYOSURGICAL DELIVERY SYSTEM (MODIFICATION) | GEH | 1996-02-08 | 136 |
| K944221 | VERRUCA-FREEZE(TM) CRYOSURGICAL DELIVERY SYST, MODIFIED | GEH | 1994-12-15 | 122 |
Recalls
openFDA lists no recalls under a recalling firm named Cryosurgery, Inc..
Recalling firms are matched to this applicant name by name only (same normalization), so related entities that recall under another name are not counted. A recall count says nothing about how safe one company's devices are compared with another's.
Frequently asked questions
How many FDA 510(k) clearances are listed under Cryosurgery, Inc.?
FDA lists 9 510(k) clearances under the applicant name “Cryosurgery, Inc.” (first 1994, latest 2026), across 2 product codes in 2 review panels. Filings under other applicant names, such as subsidiaries, are not included.
How long has FDA taken to clear 510(k)s filed by Cryosurgery, Inc.?
The median time from FDA receipt to decision across 510(k)s cleared under the name Cryosurgery, Inc. is 107 days. Since 2017: 48 days, versus 93 days for all cleared 510(k)s in the same product codes.
Which FDA product codes appear under Cryosurgery, Inc.?
The most frequent FDA product codes under this applicant name are GEH (Unit, Cryosurgical, Accessories, 8); MLY (Vapocoolant Device, 1).
Next steps
- See all 9 Cryosurgery, Inc. clearances with predicates and recalls
- Run predicate analysis for product code GEH, Cryosurgery, Inc.'s most frequent
Data from openFDA (510(k), PMA, De Novo, device recalls), ClinicalTrials.gov and SEC company tickers. Each page covers one FDA applicant name, with punctuation and legal suffixes removed; filings under other names are not included. Review days run from FDA receipt to decision. Not regulatory advice. Report an error in this data.