FDA applicant
Crystal Medical Technology
FDA records 2 decisions for Crystal Medical Technology (Birmingham, AL) from 1996 to 1998: 2 510(k) clearances. All are in product code DZE (Implant, Endosseous, Root-Form). Its devices cite 11 predicates, 1 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 Crystal Medical Technology’s devices, and how often a recall has named them.
FDA decisions per year
No FDA decision for Crystal Medical Technology since 2007.
Recalls per year
No recall linked to its devices since 2007.
Planning a device like Crystal Medical Technology’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 “Crystal”
FDA records each applicant name separately; these may or may not be the same firm.