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Histofreezer

CRYOCONCEPTS, LP · Model 1001-0336 · UDI-DI 00850077006111

GEH Prescription
1
510(k) clearances
3,252
Adverse events (57 deaths)
106
Recalls
109
Facilities

Description

Histofreezer, Kit, U.S., 5M1C The Histofreezer Portable Cryosurgical System is used for the removal of warts and other benign skin lesions: Genital Lesions, Molluscum Contagiosum, Seborrheic Keratoses, Skin Tags, Verruca Plantaris, Verruca Vulgaris, Verruca Plana, Actinic Keratoses (Facial and Non-Facial), and Lentigo (Facial and Non-Facial). The Histofreezer System should only be supplied to and used by medically trained healthcare professionals.

Recalls

DateFirmReason
2026-06-26Erbe USA IncA strong pull on the high-pressure transfer hose of cryosurgical unit may lead to pneumatic short circuit between he gas inlet and the connector resulting in CO2 leaking into the
2026-02-12Erbe USA IncProbes may rupture/burst during activation
2026-02-12Erbe USA IncProbes may rupture/burst during activation
2026-02-12Erbe USA IncProbes may rupture/burst during activation
2025-08-18Boston Scientific CorporationCertain desiccant tube subassemblies were built with end caps that were not correctly tightened.
2025-08-18Boston Scientific CorporationCertain desiccant tube subassemblies were built with end caps that were not correctly tightened.
2025-03-24Boston Scientific CorporationBoston Scientific has identified that IceSeedTM CX needles manufactured between April 2024 and February 2025 have been programmed with DEMO settings instead of Commercial settings
2025-03-24Boston Scientific CorporationBoston Scientific has identified that IceSeedTM CX needles manufactured between April 2024 and February 2025 have been programmed with DEMO settings instead of Commercial settings
2025-03-24Boston Scientific CorporationBoston Scientific has identified that IceSeedTM CX needles manufactured between April 2024 and February 2025 have been programmed with DEMO settings instead of Commercial settings
2025-03-24Boston Scientific CorporationBoston Scientific has identified that IceSeedTM CX needles manufactured between April 2024 and February 2025 have been programmed with DEMO settings instead of Commercial settings

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Data compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.