Atlas FDA

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

Bausch and Lomb, Incorporated — Predicate Candidate Screening

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

K-numberDeviceApplicantDecidedReview daysRecalls (K-match)
K252052Stellaris Elite™ vision enhancement system (BL11145, BL14455Bausch and Lomb, Incorporated2026-03-252670
K240169Stellaris Elite vision enhancement system (BL11145, BL14455,Bausch and Lomb, Incorporated2024-07-261860
K180319Bausch + Lomb Boston Advance Cleaner, Bausch + Lomb Boston ABausch and Lomb, Incorporated2018-03-27500

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