Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field. in ChinaLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field.. FDA records under its name, each linked to the record.
As of Nov 15, 2026, FDA's public records list Guangzhou Xinbo Electronic Co., Ltd. with 12 510(k) clearances. The most recent is a 510(k) clearance dated May 16, 2024: Pain Therapy Device(Model: P.T.S-X).
Drug approvals, 510(k) clearances, recalls and letters, 2017 to 2026 to date
A hatched bar is a year that is not over, so its count covers only part of the year.
| May 16, 2024 | Pain Therapy Device(Model: P.T.S-X)K230711 · NGX | 510(k) clearances |
| Mar 11, 2024 | Pain Therapy Device (Model: P.T.S-VI, P.T.S-VII)K231789 · NGX | 510(k) clearances |
| Aug 9, 2023 | Conductive Silicone Rubber ElectrodeK231167 · GXY | 510(k) clearances |
| Aug 9, 2023 | Conductive carbon film electrodeK231164 · GXY | 510(k) clearances |
| Nov 12, 2021 | DR-HO's Back Pain Relief System Pro (Models BPRS-I and BPRS-II)K202671 · NUH | 510(k) clearances |
| Nov 1, 2021 | 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)K212948 · NGX | 510(k) clearances |
| Aug 16, 2021 | Metallic Fabric ElectrodesK202636 · GXY | 510(k) clearances |
| Jul 15, 2021 | Pain Therapy DeviceK202638 · NGX | 510(k) clearances |
Spellings are joined only when they reduce to the same name, or a reviewed source names the same company. Sharing an FDA establishment number (FEI) is not enough: contract sites make products for many firms. Facts marked AI were labelled by a language model from the firm's FDA names; everything else comes from FDA or Wikidata. How this page is built
