FDA applicant

Alliance Medical Marketinig

Jacksonville Beach, FL1 decision1994–19940 recalls

FDA records 1 decision for Alliance Medical Marketinig (Jacksonville Beach, FL) in 1994: 1 510(k) clearance. All are in product code HLQ (Keratoscope, Ac-Powered). 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, ophthalmic panel, where it files most

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

FDA decisions per year

No FDA decision for Alliance Medical Marketinig since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Other applicant names beginning “Alliance”

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

Alliance Medical Corp. 47 Alliance Rubber Products Sdn. Bhd. 12 Alliance Partners, LLC 10 Alliance Pharmaceutical Corp. 2 Alliance International Co., Ltd. 2 Alliance Global Technology Co., Ltd. 2 Alliance Medical Technologies, Inc. 1 Alliance Instruments 1 Alliance Global 1 Alliance Tech Medical, Inc. 1

Alliance Medical Marketinig

Which product codes does it file in?

Who builds on its devices?

Which of its devices are cited most?

What has FDA decided for it lately?

Other applicant names beginning “Alliance”