FDA applicant

Conmed Integrated Systems (Cmis)

Beaverton, OR5 decisions2003–20090 recalls

FDA records 5 decisions for Conmed Integrated Systems (Cmis) (Beaverton, OR) from 2003 to 2009: 5 510(k) clearances. Most are in product codes GCJ (Laparoscope, General & Plastic Surgery) and FSY (Light, Surgical, Ceiling Mounted). Its devices cite 15 predicates, 4 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, gastroenterology and urology panel, where it files most

How often FDA has decided Conmed Integrated Systems (Cmis)’s devices, and how often a recall has named them.

FDA decisions per year

1in 2009

2007high 1 (2009) · low 0 (2007)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Conmed Integrated Systems (Cmis)’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 Endoscopic Technologies, Inc. 2 Conmed Electrosurgery 1 Conmed Corporation, Largo 1 Conmed Integrated Systems, Canada, Ulc 1 Conmed Linvatec Biomaterials 1

Conmed Integrated Systems (Cmis)

Which product codes does it file in?

Whose devices does it build on?

Which of its devices are cited most?

What has FDA decided for it lately?

Other applicant names beginning “Conmed”