FDA applicant

Cameron-Miller, Inc.

Mchenry, IL14 decisions1977–19940 recalls

FDA records 14 decisions for Cameron-Miller, Inc. (Mchenry, IL) from 1977 to 1994: 14 510(k) clearances. Most are in product codes GEI (Electrosurgical, Cutting & Coagulation &…) and HGI (Electrocautery, Gynecologic (And Accessories)). 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 Cameron-Miller, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Cameron-Miller, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Cameron-Miller, 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 “Cameron-Miller”

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

Cameron Medical Corp. 1

Cameron-Miller, Inc.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Cameron-Miller”