Atlas FDA

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

Owens Industries, Inc. — Predicate Candidate Screening

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

K-numberDeviceApplicantDecidedReview daysRecalls (K-match)
K926596OWENS ENDOSCOPIC INSTRUMENTS AND ACCESSORIESOwens Industries, Inc.1994-06-106390
K926594OWENS LAPAROSCOPY INSTRUMENTS AND ACCESSORIESOwens Industries, Inc.1994-06-066350
K926595OWENS BIOPSY FORCEPSOwens Industries, Inc.1994-05-256230
K932796OWENS TROCAROwens Industries, Inc.1994-02-022380

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