FDA applicant

Micromedical Devices, Inc.

Castle Pines Village, CO7 decisions1984–20040 recalls

FDA records 7 decisions for Micromedical Devices, Inc. (Castle Pines Village, CO) from 1984 to 2004: 7 510(k) clearances. Most are in product codes GCJ (Laparoscope, General & Plastic Surgery) and DRO (Pacemaker, Cardiac, External Transcutaneous…). Its devices cite 1 predicate, 0 of them its own earlier devices. 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, gastroenterology and urology panel, where it files most

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

FDA decisions per year

No FDA decision for Micromedical Devices, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Micromedical Devices, 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 “Micromedical”

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

Micromedical, Inc. 7 Micromedical Industries, Ltd. 6 Micromedical Technologies, Inc. 5

Micromedical Devices, Inc.

Which product codes does it file in?

Whose devices does it build on?

Who builds on its devices?

Which of its devices are cited most?

What has FDA decided for it lately?

Other applicant names beginning “Micromedical”