510(k) Report

FDA applicant

Micron Surgical, Inc.

Margate, FL1 decision2001–20010 recalls

FDA records 1 decision for Micron Surgical, Inc. (Margate, FL) in 2001: 1 510(k) clearance. All are in product code HMX (Cannula, Ophthalmic). 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 Micron Surgical, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Micron Surgical, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Micron Surgical, 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

Other applicant names beginning “Micron”

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