Guangzhou Xinbo Electronic Co., Ltd.
FDA Regulatory Profile
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 12
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|
| K230711 | Pain Therapy Device(Model: P.T.S-X) | May 16, 2024 |
| K231789 | Pain Therapy Device (Model: P.T.S-VI, P.T.S-VII) | March 11, 2024 |
| K231167 | Conductive Silicone Rubber Electrode | August 9, 2023 |
| K231164 | Conductive carbon film electrode | August 9, 2023 |
| K202671 | DR-HO's Back Pain Relief System Pro (Models BPRS-I and BPRS-II) | November 12, 2021 |
| K212948 | Pain Therapy Device(Model: DH-P.T.S-I, DH-P.T.S-II, DH-P.T.S-IIA, DH-P.T.S-IIB, DH-CP-I) | November 1, 2021 |
| K202636 | Metallic Fabric Electrodes | August 16, 2021 |
| K202638 | Pain Therapy Device | July 15, 2021 |
| K200402 | DR-HO'S Electro Therapy Conductive Gel | November 25, 2020 |
| K190118 | Dr-Ho's Foot Pad Electrode (Models: DHFRE-I, CP-I, CP-II, CP-III) | May 13, 2020 |
| K172887 | XinBo Electrode (Model: Neck Therapy Pro - I, Neck Therapy Pro - II, Neck Therapy Pro - III, Neck Th | April 19, 2018 |
| K163611 | Pain Therapy Device | September 19, 2017 |