FDA applicant

M&M Dental Studio, Inc.

New York, NY1 decision2015–20150 recalls

FDA records 1 decision for M&M Dental Studio, Inc. (New York, NY) in 2015: 1 510(k) clearance. All are in product code EJX (Anchor, Preformed). 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 M&M Dental Studio, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

1in 2015

2015high 1 (2015) · low 0 (2016)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2015.

FIG. 1 — M&M Dental Studio, Inc. by year, 2015–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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M&M Dental Studio, Inc.

Which product codes does it file in?

What has FDA decided for it lately?