Atlas FDA

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

EKB — Predicate Candidate Screening

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

K-numberDeviceApplicantDecidedReview daysRecalls (K-match)
K8517241410/1 TO 1435/13 VARIOUS PROBES & EXPLORERSArtiberia1985-07-02680
K823914EXPLORER TIPTreace Medical, Inc.1983-01-21240
K821780BEACH EXPLORER NO. 23T.G.Pacific Dental Corp.1982-07-06190

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