Predicate Research Report · generated 2026-08-22 · Print / save as PDF · Save to account
Hony Medical Co., Ltd. · Predicate Candidate Screening
4 FDA 510(k) clearances under this manufacturer; the 50 most recent screened below.
| K-number | Device | Applicant | Decided | Review days | Recalls (K-match) |
|---|---|---|---|---|---|
| K241789 | Non-Sterile Ultrasound Transmission Gels | Hony Medical Co., Ltd. | 2024-07-24 | 33 | 0 |
| K241615 | Transducer Probe Cover | Hony Medical Co., Ltd. | 2024-07-03 | 28 | 0 |
| K221278 | Transducer Probe Cover | Hony Medical Co., Ltd. | 2023-01-11 | 253 | 0 |
| K221999 | Ultrasound Transmission Gels | Hony Medical Co., Ltd. | 2022-08-30 | 54 | 0 |
Methodology
Recall counts reflect FDA recall records explicitly referencing each K-number; FDA links recalls to K-numbers inconsistently, so 0 means "none found in FDA records," not "never recalled." Data: FDA openFDA, refreshed weekly. Verify decisions of consequence against the primary source. Full candidate set and CSV export: atlasbyauro.com.
Prepared with Atlas
Predicate research, review-time statistics and recall monitoring for 510(k) teams: atlasbyauro.com/fda