FDA applicant
Kendall Research Center
FDA records 14 decisions for Kendall Research Center (Mchenry, IL) from 1976 to 1980: 14 510(k) clearances. Most are in product codes NAB (Gauze / Sponge,Nonresorbable For External Use) and CAZ (Anesthesia Conduction Kit). 2 recalls are linked to its devices, 1 Class I.
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) refreshed weekly
How often FDA has decided Kendall Research Center’s devices, and how often a recall has named them.
FDA decisions per year
No FDA decision for Kendall Research Center since 2007.
Recalls per year
1in 2023
Class I Class II/III not classified
Planning a device like Kendall Research Center’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 “Kendall”
FDA records each applicant name separately; these may or may not be the same firm.