510(k) Report

FDA applicant

Crystal Medical Technology

Birmingham, AL2 decisions1996–19980 recalls

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, last Nov 3, 2026

FIG. A — Illustration, dental panel, where it files most

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.

FIG. 1 — Crystal Medical Technology by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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.

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Other applicant names beginning “Crystal”

FDA records each applicant name separately; these may or may not be the same firm.