Medical device makerLabelled 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 Jkh Health Co., Ltd. with 10 510(k) clearances. The most recent is a 510(k) clearance dated Oct 24, 2025: Cryon-X Cold Compression.
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.
| Oct 24, 2025 | Cryon-X Cold CompressionK253150 · IRP | 510(k) clearances |
| Jun 4, 2025 | Ultrasound StimulatorK240788 · IMI | 510(k) clearances |
| May 1, 2024 | Cold CompressionK240986 · IRP | 510(k) clearances |
| Feb 23, 2024 | Lymphedema CompressionK240011 · JOW | 510(k) clearances |
| Oct 27, 2023 | Cold/Hot CompressionK223541 · IRP | 510(k) clearances |
| Nov 28, 2022 | Infrared Thermometer, Model: JKH-300, JKH-301, JKH-302, JKH-303, JKH-304K211050 · FLL | 510(k) clearances |
| Jan 21, 2021 | Overlapped Compression TherapyK202839 · JOW | 510(k) clearances |
| Jul 1, 2020 | StimPlus Patch, StimPlus Patch, StimPlus PatchK200561 · NUH | 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
