FDA applicant

Consolidated Medical Equipment, Inc.

Utica, NY15 decisions1980–19860 recalls

FDA records 15 decisions for Consolidated Medical Equipment, Inc. (Utica, NY) from 1980 to 1986: 15 510(k) clearances. Most are in product codes GEI (Electrosurgical, Cutting & Coagulation &…) and GXY (Electrode, Cutaneous). 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 Consolidated Medical Equipment, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Consolidated Medical Equipment, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Consolidated Medical Equipment, Inc.’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 “Consolidated”

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

Consolidated Technologies, Inc. 20 Consolidated Products & Services, Inc. 7 Consolidated Technology 4 Consolidated Research of Richmond, Inc. 2 Consolidated Stores Corp. 2 Consolidated Machine Corp. 2 Consolidated Technologies of Wisconsin 2 Consolidated Research of Richmond, Inc. Dba General… 1 Consolidated Stores Intl. Corp. 1 Consolidated Industries of Greater Syracuse, Inc. 1 Consolidated Health & Sports Prod. 1 Consolidated Radiation Services, Inc. 1

Consolidated Medical Equipment, Inc.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Consolidated”