Atlas FDA

Predicate Research Report · generated 2026-08-23 · Print / save as PDF · Save to account

Sandstone Medical (Suzhou), Inc. · Predicate Candidate Screening

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

K-numberDeviceApplicantDecidedReview daysRecalls (K-match)
K252908Easydrip Classic Pen Needle; Easydrip Plus Pen Needle; EasydSandstone Medical (Suzhou), Inc.2026-03-251940
K210864Safety Pen NeedleSandstone Medical (Suzhou), Inc.2022-02-173310
K193422Easydrip Pen Needle, Easydrip Plus Pen NeedleSandstone Medical (Suzhou), Inc.2021-02-024210

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