FDA applicant
Medical Innovation, Ltd.
FDA records 1 decision for Medical Innovation, Ltd. (Washington, DC) in 1998: 1 510(k) clearance. All are in product code MEG (Syringe, Antistick). 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 Medical Innovation, Ltd.’s devices, and how often a recall has named them.
FDA decisions per year
No FDA decision for Medical Innovation, Ltd. since 2007.
Recalls per year
No recall linked to its devices since 2007.
Planning a device like Medical Innovation, Ltd.’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