Atlas FDA

Predicate Research Report · generated 2026-08-22 · Print / save as PDF · Save to account

Vinno Technology (Suzhou) Co.,Ltd · Predicate Candidate Screening

6 FDA 510(k) clearances under this manufacturer; the 50 most recent screened below.

174 daysmedian FDA review time
364 days90th percentile
6clearances measured
K-numberDeviceApplicantDecidedReview daysRecalls (K-match)
K240676ULTIMUS Series Ultrasound Diagnostic SystemVinno Technology (Suzhou) Co.,Ltd2024-12-162800
K230160VINNO G86,VINNO G86E,VINNO G65,VINNO G65P,VINNO G65E,VINNO GVinno Technology (Suzhou) Co.,Ltd2023-06-231550
K223917VINNO E20, VINNO E10,VINNO E10P,VINNO E10E, VINNO X1,VINNO XVinno Technology (Suzhou) Co.,Ltd2023-06-171700
K223920VINNO G50, VINNO G55, VINNO M50, VINNO E30, VINNO X5, VINNO Vinno Technology (Suzhou) Co.,Ltd2023-06-171700
K221911VINNO 6PRO, VINNO 6EXP, VINNO 5PRO, VINNO 5EXP, VINNO 3, VINVinno Technology (Suzhou) Co.,Ltd2022-12-211740
K190120VINNO 8, VINNO 6, VINNO 5Vinno Technology (Suzhou) Co.,Ltd2020-01-233640

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