FDA applicant
Imm Enterprises, Ltd.
FDA records 52 decisions for Imm Enterprises, Ltd. (Mchenry, IL) from 1983 to 1984: 52 510(k) clearances. Most are in product codes HTD (Forceps) and KOA (Surgical Instruments, G-U, Manual (And…). 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 Imm Enterprises, Ltd.’s devices, and how often a recall has named them.
FDA decisions per year
No FDA decision for Imm Enterprises, Ltd. since 2007.
Recalls per year
No recall linked to its devices since 2007.
Planning a device like Imm Enterprises, Ltd.’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.
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