FDA applicant
BunkerHill Health
FDA records 8 decisions for BunkerHill Health (San Francisco, CA) from 2024 to 2026: 8 510(k) clearances. Most are in product codes JAK (System, X-Ray, Tomography, Computed) and QIH (Automated Radiological Image Processing Software). Since 2016 its 510(k)s took a median of 202 days from receipt to decision, against 153 for FDA’s reviews in the same codes and years. Its devices cite 9 predicates, 3 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 BunkerHill Health’s devices, and how often a recall has named them.
FDA decisions per year
5in 2025
2026 so far, outlined.
Recalls per year
No recall linked to its devices since 2024.
Planning a device like BunkerHill Health’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 “BunkerHill”
FDA records each applicant name separately; these may or may not be the same firm.