FDA applicant
The Institute For Radiological Image Sciences, Inc.
FDA records 1 decision for The Institute For Radiological Image Sciences, Inc. (Germantown, MD) in 1990: 1 510(k) clearance. All are in product code KGI (Densitometer, Bone). 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 The Institute For Radiological Image Sciences, Inc.’s devices, and how often a recall has named them.
FDA decisions per year
No FDA decision for The Institute For Radiological Image Sciences, Inc. since 2007.
Recalls per year
No recall linked to its devices since 2007.
Planning a device like The Institute For Radiological Image…’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 “The”
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