FDA applicant

Micrins Surgical, Inc.

Lake Forest, IL6 decisions1987–20000 recalls

FDA records 6 decisions for Micrins Surgical, Inc. (Lake Forest, IL) from 1987 to 2000: 6 510(k) clearances. Most are in product codes EPT (Microscope, Surgical) and HXK (Holder, Needle; Orthopedic). 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 Micrins Surgical, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

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

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Micrins 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 “Micrins”

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

Micrins, Ltd. 2

Micrins Surgical, Inc.

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 “Micrins”