Predicate Research Report · generated 2026-08-23 · Print / save as PDF · Save to account
Foshan Cicada Dental Instrument 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) |
|---|---|---|---|---|---|
| K202075 | Dental Electric Motor | Foshan Cicada Dental Instrument Co, Ltd. | 2022-03-11 | 592 | 0 |
| K192649 | Endo Motor | Foshan Cicada Dental Instrument Co, Ltd. | 2021-03-12 | 535 | 0 |
| K192233 | LED Curing Light | Foshan Cicada Dental Instrument Co, Ltd. | 2020-02-13 | 178 | 0 |
| K181900 | Dental high speed handpiece, Dental low speed handpiece | Foshan Cicada Dental Instrument Co, Ltd. | 2019-12-09 | 511 | 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