FDA applicant

Steris C/O Medical Device Consultants, Inc.

North Attleboro, MA1 decision1988–19883 recalls

FDA records 1 decision for Steris C/O Medical Device Consultants, Inc. (North Attleboro, MA) in 1988: 1 510(k) clearance. All are in product code MED (Sterilant, Medical Devices). 3 recalls are 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 hospital panel, where it files most

How often FDA has decided Steris C/O Medical Device Consultants, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Steris C/O Medical Device Consultants, Inc. since 2007.

Recalls per year

1in 2008

2007high 1 (2008) · low 0 (2007)2026

Class I Class II/III not classified

FIG. 1 — Steris C/O Medical Device Consultants, 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 “Steris”

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

STERIS Corporation 228 Steris Corporations 7 Steris Corparation 2

Steris C/O Medical Device Consultants, 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?

What has been recalled?

Other applicant names beginning “Steris”