FDA applicant
King & Spalding
FDA records 7 decisions for King & Spalding (Washington, DC) from 1994 to 1995: 7 510(k) clearances. Most are in product codes LZK (Implant, Malar) and DXN (System, Measurement, Blood-Pressure…). 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 & Spalding’s devices, and how often a recall has named them.
FDA decisions per year
No FDA decision for King & Spalding since 2007.
Recalls per year
No recall linked to its devices since 2007.
Planning a device like King & Spalding’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”
FDA records each applicant name separately; these may or may not be the same firm.