Atlas FDA

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

Lever Brothers Company, Inc. · Predicate Candidate Screening

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

K-numberDeviceApplicantDecidedReview daysRecalls (K-match)
K850610PEPSODENT DENTURE ADHESIVE CREAMLever Brothers Company, Inc.1985-05-15890
K851182PEPSODENT DENTURE CLEANSER-WESTONE FORMULALever Brothers Company, Inc.1985-04-29340
K851183PEPSODENT DENTURE CLEANSER PDP FORMULALever Brothers Company, Inc.1985-04-29340
K781018DX TOOTHBRUSHLever Brothers Company, Inc.1978-06-30140

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