FDA applicant

Generic Medical, Inc.

Alpharetta, GA1 decision1995–19950 recalls

FDA records 1 decision for Generic Medical, Inc. (Alpharetta, GA) in 1995: 1 510(k) clearance. All are in product code DXQ (Blood Pressure Cuff). 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, cardiovascular panel, where it files most

How often FDA has decided Generic Medical, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Generic Medical, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Other applicant names beginning “Generic”

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

Generic Medical Device, Inc. 4 Generic Medical Devices, Inc. 1 Generic Laboratory, Ltd. 1

Generic Medical, Inc.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Generic”