FDA applicant
Novus Technologies, Inc.
FDA records 1 decision for Novus Technologies, Inc. (San Leandro, CA) in 1994: 1 510(k) clearance. All are in product code LMB (Device, Digital Image Storage, Radiological). 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 Novus Technologies, Inc.’s devices, and how often a recall has named them.
FDA decisions per year
No FDA decision for Novus Technologies, Inc. since 2007.
Recalls per year
No recall linked to its devices since 2007.
Planning a device like Novus Technologies, Inc.’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 “Novus”
FDA records each applicant name separately; these may or may not be the same firm.