FDA applicant

Conmed Integrated Systems, Canada, Ulc

Largo, FL1 decision2006–20060 recalls

FDA records 1 decision for Conmed Integrated Systems, Canada, Ulc (Largo, FL) in 2006: 1 510(k) clearance. All are in product code FYD (Apparatus, Exhaust, Surgical). Its devices cite 2 predicates, 0 of them its own earlier devices. 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 Conmed Integrated Systems, Canada, Ulc’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Conmed Integrated Systems, Canada, Ulc since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Conmed Integrated Systems, Canada, Ulc by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

Planning a device like Conmed Integrated Systems, Canada, Ulc’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 “Conmed”

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

Conmed Corporation 84 Conmed Linvatec 21 Conmed Andover Medical, Inc. 8 Conmed Integrated Systems (Cmis) 5 Conmed Endoscopic Technologies, Inc. 2 Conmed Electrosurgery 1 Conmed Corporation, Largo 1 Conmed Linvatec Biomaterials 1

Conmed Integrated Systems, Canada, Ulc

Which product codes does it file in?

Whose devices does it build on?

Who builds on its devices?

Which of its devices are cited most?

What has FDA decided for it lately?

Other applicant names beginning “Conmed”