FDA applicant
King'S Bay Intl., Inc.
FDA records 1 decision for King'S Bay Intl., Inc. (Vista, CA) in 1993: 1 510(k) clearance. All are in product code JHI (Visual, Pregnancy Hcg, Prescription Use). 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 King'S Bay Intl., Inc.’s devices, and how often a recall has named them.
FDA decisions per year
No FDA decision for King'S Bay Intl., Inc. since 2007.
Recalls per year
No recall linked to its devices since 2007.
Planning a device like King'S Bay Intl., Inc.’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 “King'S”
FDA records each applicant name separately; these may or may not be the same firm.