FDA applicant

Surgi-Quip Inc.U

Mchenry, IL8 decisions1982–19840 recalls

FDA records 8 decisions for Surgi-Quip Inc.U (Mchenry, IL) from 1982 to 1984: 8 510(k) clearances. Most are in product codes HBN (Chair, Neurosurgical) and FSE (Table, Operating-Room, Manual). 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 Surgi-Quip Inc.U’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Surgi-Quip Inc.U since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Surgi-Quip Inc.U’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 “Surgi-Quip”

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

Surgi-Vision, Inc. 9 Surgi-Med, Inc. 5 Surgi-Aid Endoscopics, Inc. 1

Surgi-Quip Inc.U

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Surgi-Quip”