Predicate Research Report · generated 2026-08-23 · Print / save as PDF · Save to account
Realton (Suzhou) Medical Technology Co., Ltd. · Predicate Candidate Screening
3 FDA 510(k) clearances under this manufacturer; the 50 most recent screened below.
| K-number | Device | Applicant | Decided | Review days | Recalls (K-match) |
|---|---|---|---|---|---|
| K202828 | Surgical Green Laser System | Realton (Suzhou) Medical Technology Co., Ltd. | 2021-06-04 | 253 | 0 |
| K202702 | FLARE Single-Use Surgical Laser Fiber | Realton (Suzhou) Medical Technology Co., Ltd. | 2021-02-26 | 163 | 0 |
| K202601 | Single-use Sterile medical laser fiber | Realton (Suzhou) Medical Technology Co., Ltd. | 2020-12-15 | 98 | 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