FDA applicant

Allied Systems Co.

Farmington, CT1 decision1990–19900 recalls

FDA records 1 decision for Allied Systems Co. (Farmington, CT) in 1990: 1 510(k) clearance. All are in product code MAV (Syringe, Balloon Inflation). 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 Allied Systems Co.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Allied Systems Co. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Allied Systems Co. by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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Other applicant names beginning “Allied”

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

Allied Healthcare Products, Inc. 26 Allied Associates, Inc. 9 Allied Biomedical Corp. 9 Allied Instrumentation Laboratory 7 Allied Signal, Inc. 2 Allied Rubber Industries Sdn. Bhd. 2 Allied Photo Products Co., Inc. 1 Allied Hill Enterprises, Ltd. 1 Allied Dental Solutions 1 Allied Medical Technologies, Inc. 1 Allied Fisher Scientific 1 Allied Advanced Technologies (Aat) 1

Allied Systems Co.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Allied”