510(k) Report

FDA applicant

Contemporary Surgical Systems, Inc.

Mchenry, IL3 decisions1979–19830 recalls

FDA records 3 decisions for Contemporary Surgical Systems, Inc. (Mchenry, IL) from 1979 to 1983: 3 510(k) clearances. Most are in product codes HMX (Cannula, Ophthalmic) and HQE (Instrument, Vitreous Aspiration And Cutting…). 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 Contemporary Surgical Systems, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Contemporary Surgical Systems, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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

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Other applicant names beginning “Contemporary”

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