FDA applicant

Micro-Medical Devices, Inc.

Castle Pines Village, CO8 decisions1994–20010 recalls

FDA records 8 decisions for Micro-Medical Devices, Inc. (Castle Pines Village, CO) from 1994 to 2001: 8 510(k) clearances. Most are in product codes HRX (Arthroscope) and KKX (Drape, Surgical, Antimicrobial). 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, general and plastic surgery panel, where it files most

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

FDA decisions per year

No FDA decision for Micro-Medical Devices, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Micro-Medical Devices, Inc.’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.

See the 510(k) Report

Micro-Medical Devices, Inc.

Which product codes does it file in?

What has FDA decided for it lately?