Cosman Medical, Inc.
United StatesFDA applicant, unverified
- Devices
- 225
- FDA recalls
- 1
What Cosman Medical, Inc. makes
Cosman Medical, Inc. manufactures radiofrequency generators and related accessories for medical procedures, including the Cosman G4 Radiofrequency Generator (Model RFG-4) and the Cosman RF Lesion Generator (Model RFG-1A). The company also produces trigeminal electrode kits such as the Cosman Tew Trigeminal Electrode Kit and Cosman Tic Trigeminal Electrode Kit, fiducial markers, RF cannulas including the Cosman CSK RF Cannula, Cosman RFK RF Cannula, and LesionPoint RF Cannula, as well as RF injection electrodes in models CU, CUR, CCD, TCD, CP, CR, and CN.
All devices manufactured by Cosman Medical, Inc. are classified as Class II medical devices and are listed in the FDA 510(k) registry. The company is based in the United States.
Catalogue
Search and filter all 225 devicesShowing 201-225 of 225
FDA recalls
FDA recall records list 1 recall initiated by Cosman Medical, Inc., initiated on 2017-07-05. By recorded status: 1 terminated. The reasons filed fall into these groups: sterility or contamination and manufacturing or quality process. A recall is often a precaution started by the manufacturer, and a count of records is not a verdict on a company.
Recalls initiated per year
- 2017 1
- 2018 0
- 2019 0
- 2020 0
- 2021 0
- 2022 0
- 2023 0
- 2024 0
- 2025 0
- 2026 0
2017
- 5 Jul 2017 Z-0687-2018 Class II Terminated After multiple reprocessing cycles, the epoxy resin which holds the TCN Electrode in the hub can exhibit signs of damage. In some cases, this damage may result in the inability to fully remove blood and/or tissue residuals prior to cleaning and re-sterilizing the device.