FDA applicant

Conmed Andover Medical, Inc.

Haverhill, MA8 decisions1994–19950 recalls

FDA records 8 decisions for Conmed Andover Medical, Inc. (Haverhill, MA) from 1994 to 1995: 8 510(k) clearances. Most are in product codes DRX (Electrode, Electrocardiograph) and DSA (Cable, Transducer And Electrode, Patient…). 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, cardiovascular panel, where it files most

How often FDA has decided Conmed Andover Medical, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Conmed Andover Medical, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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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 Integrated Systems (Cmis) 5 Conmed Endoscopic Technologies, Inc. 2 Conmed Electrosurgery 1 Conmed Corporation, Largo 1 Conmed Integrated Systems, Canada, Ulc 1 Conmed Linvatec Biomaterials 1

Conmed Andover Medical, 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 “Conmed”