Cryosurgery, Inc. is one of 16135 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Cryosurgery, Inc. - FDA 510(k) Cleared Devices
Recent clearances: FreezeSpray TA, CryoFreeze Wart and Skin Tag Remover, Verruca-Freeze H Plus
9
Total
9
Cleared
0
Denied
Cryosurgery, Inc. has 9 FDA 510(k) cleared medical devices. Based in Nashville, US.
Latest FDA clearance: Sep 2026. Active since 1994. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Cryosurgery, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Cryosurgery, Inc.
9 devices
Cleared
Sep 05, 2026
FreezeSpray TA
Physical Medicine
107d
Cleared
Oct 16, 2025
CryoFreeze Wart and Skin Tag Remover
General & Plastic Surgery
28d
Cleared
Oct 10, 2025
Verruca-Freeze H Plus
General & Plastic Surgery
29d
Cleared
Mar 13, 2025
CryoFreeze Wart and Skin Tag Remover
General & Plastic Surgery
125d
Cleared
Dec 03, 2024
Verruca-Freeze H
General & Plastic Surgery
26d
Cleared
Dec 04, 2023
Verruca-Freeze® H
General & Plastic Surgery
66d
Cleared
Jan 27, 1999
VERRUCA-FREEZE CRYOSURGERY DELIVERY SYSTEM
General & Plastic Surgery
191d
Cleared
Feb 08, 1996
VERRUCA-FREEZE CRYOSURGICAL DELIVERY SYSTEM (MODIFICATION)
General & Plastic Surgery
136d
Cleared
Dec 15, 1994
VERRUCA-FREEZE(TM) CRYOSURGICAL DELIVERY SYST, MODIFIED
General & Plastic Surgery
122d