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Cryosurgery, Inc.

United StatesFDA applicant, unverified FDA FEI 1000140327

Cryosurgery, Inc. is a medical device manufacturer, with 29 devices listed in FDA GUDID and FDA 510(k) (FDA Class II and Unclassified) as of 15 Nov 2026.

Devices
29
Registrations
FDA
FDA recalls
0

Registry facts

Counted by deviCERTS from registry records, 15 Nov 2026

Registries
  • FDA GUDID 20
  • FDA 510(k) 9

A device listed in two registries counts in both.

Device classes
  • FDA Class II 28
  • FDA Unclassified 1
Identifiers
  • FDA FEI 1000140327
  • DUNS 793483256

At a glance

Counted by deviCERTS from registry records

Market reach

United States
FDA FEI

What Cryosurgery, Inc. makes

Cryosurgery, Inc. manufactures cryosurgical systems, cryogen gases, and mechanical components designed for controlled freezing procedures. Their portfolio includes devices like the Verruca-Freeze series, intended for targeted tissue ablation, particularly for skin lesions such as verrucae (warts). These systems utilize cryogenic technology to freeze and destroy abnormal tissue while preserving surrounding healthy tissue.

The company’s devices are classified as Class II under FDA regulations and are authorised through the 510(k) pathway and the Unique Device Identifier (UDI) system. Their products are listed in the FDA’s regulatory databases, ensuring compliance with U.S. medical device standards. The manufacturer operates from the United States.

AI-generated from registry data, 3 Oct 2026. Not verified by deviCERTS or the manufacturer.

Catalogue29

Newest first, rows 1-29 of 29

Search and filter all 29 devices
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  • CryoFreeze CF-STR

    Listed Registry: GUDID Class:II
  • CryoFreeze CF-WR

    Listed Registry: GUDID Class:II
  • Verruca-Freeze H+ VFHP1M

    Active Regimes: 510(k) Registry: GUDID Class:II
  • Verruca-Freeze H+ VFHP1A

    Active Regimes: 510(k) Registry: GUDID Class:II
  • Verruca-Freeze H+ VFHP1R

    Active Regimes: 510(k) Registry: GUDID Class:II
  • Verruca-Freeze H+ VFHP2M

    Active Regimes: 510(k) Registry: GUDID Class:II
  • FreezeSpray TA Ref K261684

    Active Regimes: 510(k) Registry: 510(k) Class:—
  • Verruca-Freeze TKIT

    Active Regimes: 510(k) Registry: GUDID Class:II
  • Verruca-Freeze INTRO

    Active Regimes: 510(k) Registry: GUDID Class:II
  • Verruca-Freeze H VFH1M

    Active Regimes: 510(k) Registry: GUDID Class:II
  • Verruca-Freeze H VFH2M

    Active Regimes: 510(k) Registry: GUDID Class:II
  • Verruca-Freeze VFL300R

    Active Regimes: 510(k) Registry: GUDID Class:II
  • Verruca-Freeze VFC50

    Active Regimes: 510(k) Registry: GUDID Class:II
  • Verruca-Freeze VFC130

    Active Regimes: 510(k) Registry: GUDID Class:II
  • Verruca-Freeze VFL200R

    Active Regimes: 510(k) Registry: GUDID Class:II
  • Verruca-Freeze VFC65

    Active Regimes: 510(k) Registry: GUDID Class:II
  • Verruca-Freeze VFK65

    Active Regimes: 510(k) Registry: GUDID Class:II
  • Verruca-Freeze H VFH1A

    Active Regimes: 510(k) Registry: GUDID Class:II
  • Verruca-Freeze VFK50

    Active Regimes: 510(k) Registry: GUDID Class:II
  • Verruca-Freeze H VFH1R

    Active Regimes: 510(k) Registry: GUDID Class:II
  • Verruca-Freeze VFL100

    Active Regimes: 510(k) Registry: GUDID Class:II
  • Verruca-Freeze Cryosurgery Delivery System Ref K982506

    Active Regimes: 510(k) Registry: 510(k) Class:II
  • CryoFreeze Wart and Skin Tag Remover Ref K243487

    Active Regimes: 510(k) Registry: 510(k) Class:II
  • Verruca-Freeze H Ref K243454

    Active Regimes: 510(k) Registry: 510(k) Class:II
  • Verruca-Freeze® H Ref K233347

    Active Regimes: 510(k) Registry: 510(k) Class:II
  • Verruca-Freeze H Plus Ref K252903

    Active Regimes: 510(k) Registry: 510(k) Class:II
  • CryoFreeze Wart and Skin Tag Remover Ref K253000

    Active Regimes: 510(k) Registry: 510(k) Class:II
  • Verruca-Freeze(Tm) Cryosurgical Delivery Syst, Modified Ref K944221

    Active Regimes: 510(k) Registry: 510(k) Class:II
  • Verruca-Freeze Cryosurgical Delivery System (Modification) Ref K955083

    Active Regimes: 510(k) Registry: 510(k) Class:II

Rows 1-29 of 29

Company details

FDA FEI number
1000140327
DUNS number
793483256
Address
5829 OLD HARDING PIKE, NASHVILLE, TN, 37205
Phone
+1 (615) 354-0414

Frequently asked questions

How many devices does Cryosurgery, Inc. have in the registry?

The registry currently lists 29 devices for Cryosurgery, Inc.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Cryosurgery, Inc.'s devices?

Among its 29 most recently registered devices, Cryosurgery, Inc. has devices listed in FDA 510(k) (9 devices) and FDA GUDID (20 devices). A device can be listed in more than one registry, so these counts overlap.

What risk classes do Cryosurgery, Inc.'s devices fall under?

Among its 29 most recently registered devices, the classes recorded for Cryosurgery, Inc.'s devices are Class II. Each device page shows its own class and authorisation.

What are the newest devices from Cryosurgery, Inc. in the registry?

The most recently registered devices listed for Cryosurgery, Inc. include CryoFreeze CF-STR, CryoFreeze CF-WR, Verruca-Freeze H+ VFHP1M and Verruca-Freeze H+ VFHP1A.

Generated automatically from registry data and not verified by a human reviewer.