FDA applicant
Biological Corp. of America
FDA records 6 decisions for Biological Corp. of America (Mchenry, IL) from 1976 to 1982: 6 510(k) clearances. Most are in product codes KSG (Media, Potentiating For In Vitro Diagnostic Use) and KSK (Solution, Stabilized Enzyme). 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 Biological Corp. of America’s devices, and how often a recall has named them.
FDA decisions per year
No FDA decision for Biological Corp. of America since 2007.
Recalls per year
No recall linked to its devices since 2007.
Planning a device like Biological Corp. of America’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 “Biological”
FDA records each applicant name separately; these may or may not be the same firm.