Shenzhen Konmed Technology Co., Ltd.
FDA Regulatory Profile
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 6
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|
| K233576 | Konmed Incontinence Stimulation Electrode (Vaginal Probe: KM-503, KM-504, KM-505, KM-506, KM-507, KM | February 23, 2024 |
| K220161 | Biofeedback Nerve and Muscle Stimulator | July 20, 2022 |
| K202648 | Biofeedback Nerve and Muscle Stimulator | December 8, 2020 |
| K163288 | Pelvifine Pelvic Muscle Trainer | January 18, 2018 |
| K171722 | Electrodes with snap / Electrodes with pigtail | January 10, 2018 |
| K171721 | Electrodes with silver conductive | January 5, 2018 |