FDA applicant
Nanopass Technologies, Ltd.
FDA records 1 decision for Nanopass Technologies, Ltd. (Washington, DC) in 2010: 1 510(k) clearance. All are in product code FMI (Needle, Hypodermic, Single Lumen). Its devices cite 3 predicates, 0 of them its own earlier devices. 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 Nanopass Technologies, Ltd.’s devices, and how often a recall has named them.
FDA decisions per year
1in 2010
2026 so far, outlined.
Recalls per year
No recall linked to its devices since 2010.
Planning a device like Nanopass Technologies, 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