CRYOPEN CRYOSURGICAL SYSTEM, K102214— 510(k) K110754

Substantially Equivalent

Cryopen, Inc.

FDA 510(k) clearance K110754 for CRYOPEN CRYOSURGICAL SYSTEM, K102214, Substantially Equivalent on 2011-09-09. Applicant: Cryopen, Inc..

Clearance details

Applicant: Cryopen, Inc.
Product code: Code GEH
Advisory panel: General, Plastic Surgery
Date received: 2011-03-18
Decision date: 2011-09-09
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Southlake, TX, US

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Adverse events under product code GEH

product code GEH

Death: 25
Injury: 351
Malfunction: 901
Total: 1,277

Source: openFDA MAUDE database, 2020-01-01 through 2026-04-23. Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →

Data sourced from openFDA. This site is unofficial and independent of the FDA.