FDA applicant

The Medical Group, Inc.

Reno, NV16 decisions1986–19912 recalls

FDA records 16 decisions for The Medical Group, Inc. (Reno, NV) from 1986 to 1991: 16 510(k) clearances. Most are in product codes EAX (Mirror, Mouth) and EFQ (Gauze/Sponge, Internal). 2 recalls are 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 The Medical Group, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for The Medical Group, Inc. since 2007.

Recalls per year

2in 2013

2007high 2 (2013) · low 0 (2007)2026

Class I Class II/III not classified

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

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The Medical Group, Inc.

Which product codes does it file in?

What has FDA decided for it lately?

What has been recalled?