FDA applicant
Alliance Medical Corp.
FDA records 47 decisions for Alliance Medical Corp. (Phoenix, AZ) from 1994 to 2007: 47 510(k) clearances. Most are in product codes NLH (Catheter, Recording, Electrode, Reprocessed) and KTT (Appliance, Fixation, Nail/Blade/Plate…). Its devices cite 155 predicates, 11 of them its own earlier devices. 48 recalls are linked to its devices.
FDA’s records also spell it “Alliance Medical, Inc.”.
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) refreshed weekly
How often FDA has decided Alliance Medical Corp.’s devices, and how often a recall has named them.
FDA decisions per year
1in 2007
2026 so far, outlined.
Recalls per year
27in 2026
Class I Class II/III not classified
Planning a device like Alliance Medical Corp.’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 “Alliance”
FDA records each applicant name separately; these may or may not be the same firm.