Shenzhen Kentro Medical Electronics Co., Ltd.
FDA Regulatory Profile
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 10
- Inspections
- 1
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|
| K242332 | Transcutaneous Electronic Nerve Stimulator (KTR-2301, KTR-2302, KTR-2341, KTR-2342, KTR-2401, KTR-2 | November 5, 2024 |
| K232517 | Transcutaneous Electrical Nerve Stimulator For Pain Relief (Model: KTR-2302, KTR-2401, KTR-2402, KTR | December 8, 2023 |
| K222870 | Transcutaneous Electrical Nerve Stimulator, Model: KTR-4031, KTR-4032, KTR-4012, KTR-4015, KTR-4029, | May 10, 2023 |
| K220998 | Transcutaneous Electrical Nerve Stimulator, Model: KTR-405 | August 24, 2022 |
| K200177 | Low-frequency Multi-function physiotherapy instrument | March 25, 2021 |
| K200237 | Transcutaneous Electronic Nerve Stimulator | October 19, 2020 |
| K191982 | Low-Frequency Multi-function Physiotherapy Instrument (Model: KTR-2230, KTR-2220, KTR-2210, KTR-2231 | September 25, 2020 |
| K183288 | Transcutaneous Electrical Nerve Stimulator | July 30, 2019 |
| K181728 | Muscle Trainer | October 17, 2018 |
| K170205 | Low-Frequency Therapy Instrument /Model: KTR-201, KTR-202, KTR-203 | May 11, 2017 |