FDA applicant
Hillwood Corp.
FDA records 1 decision for Hillwood Corp. (Mchenry, IL) in 1978: 1 510(k) clearance. All are in product code GJG (Pipette, Quantitative, Hematology). 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 Hillwood Corp.’s devices, and how often a recall has named them.
FDA decisions per year
No FDA decision for Hillwood Corp. since 2007.
Recalls per year
No recall linked to its devices since 2007.
Planning a device like Hillwood Corp.’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) Report