510(k) Report

FDA applicant

Multi Media Dental Systems, Inc.

Roswell, GA1 decision2000–20000 recalls

FDA records 1 decision for Multi Media Dental Systems, Inc. (Roswell, GA) in 2000: 1 510(k) clearance. All are in product code MUH (System, X-Ray, Extraoral Source, Digital). 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 Multi Media Dental Systems, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Multi Media Dental Systems, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Multi Media Dental Systems, Inc. by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

Planning a device like Multi Media Dental Systems, Inc.’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 “Multi”

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