Predicate Research Report · generated 2026-08-22 · Print / save as PDF · Save to account
Kaycor Intl., Ltd. — Predicate Candidate Screening
7 FDA 510(k) clearances under this manufacturer; the 50 most recent screened below.
43 daysmedian FDA review time
167 days90th percentile
7clearances measured
| K-number | Device | Applicant | Decided | Review days | Recalls (K-match) |
|---|---|---|---|---|---|
| K965072 | PANOURA ULTRA PAN AND PANOURA ULTRA PAN/CEPH PANORAMIC/CEPHA | Kaycor Intl., Ltd. | 1997-01-27 | 39 | 0 |
| K931717 | YOSHIDA/KAYCOR X-707 WALL MOUNTED DENTAL X-RAY | Kaycor Intl., Ltd. | 1993-09-20 | 167 | 0 |
| K832063 | ROBIN CORDLESS HANDPIECE | Kaycor Intl., Ltd. | 1983-08-26 | 60 | 0 |
| K822740 | K30000 DENTAL CHAIR | Kaycor Intl., Ltd. | 1982-09-28 | 19 | 0 |
| K813348 | YOSHIDA RIDO-F, MODEL LM-01 | Kaycor Intl., Ltd. | 1982-01-07 | 41 | 0 |
| K811210 | YOSHIDA-PANOURA 10 | Kaycor Intl., Ltd. | 1981-08-24 | 112 | 0 |
| K811211 | YOSHIDA AP 100 | Kaycor Intl., Ltd. | 1981-06-16 | 43 | 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