FDA applicant
Johnson & Johnson Consumer Products, Inc.
FDA records 8 decisions for Johnson & Johnson Consumer Products, Inc. (Skillman, NJ) from 1984 to 2007: 8 510(k) clearances. Most are in product codes KGX (Tape And Bandage, Adhesive) and JES (Floss, Dental). Its devices cite 2 predicates, 0 of them its own earlier devices. No recall is linked to its devices.
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) refreshed weekly
How often FDA has decided Johnson & Johnson Consumer Products, Inc.’s devices, and how often a recall has named them.
FDA decisions per year
1in 2007
2026 so far, outlined.
Recalls per year
No recall linked to its devices since 2007.
Planning a device like Johnson & Johnson Consumer Products…’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.
See the 510(k) ReportOther applicant names beginning “Johnson”
FDA records each applicant name separately; these may or may not be the same firm.