FDA applicant
Mumtaz I. Malik
FDA records 7 decisions for Mumtaz I. Malik (Elizabethtown, KY) from 1988 to 1990: 7 510(k) clearances. Most are in product codes LXH (Orthopedic Manual Surgical Instrument) and LRP (Tray, Surgical). 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 Mumtaz I. Malik’s devices, and how often a recall has named them.
FDA decisions per year
No FDA decision for Mumtaz I. Malik since 2007.
Recalls per year
No recall linked to its devices since 2007.
Planning a device like Mumtaz I. Malik’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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