FDA applicant

Automated Medical Products Corp.

New York, NY6 decisions1979–19950 recalls

FDA records 6 decisions for Automated Medical Products Corp. (New York, NY) from 1979 to 1995: 6 510(k) clearances. Most are in product codes GCJ (Laparoscope, General & Plastic Surgery) and GAD (Retractor). No recall is linked to its devices.

FDA’s records also spell it “Automated Medical Products, Inc.”.

Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) refreshed weekly, last Nov 3, 2026

FIG. A — Illustration, general and plastic surgery panel, where it files most

How often FDA has decided Automated Medical Products Corp.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Automated Medical Products Corp. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Other applicant names beginning “Automated”

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

Automated Screening Devices 2 Automated IV Systems, Inc. 1 Automated Ophthalmics, Inc. 1 Automated Testing Services, Ltd. 1 Automated Lens System 1 Automated Imaging Diagnostics, LLC 1

Automated Medical Products Corp.

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 “Automated”