FDA applicant

Arbor Technologies, Inc.

Ann Arbor, MI10 decisions1986–19970 recalls

FDA records 10 decisions for Arbor Technologies, Inc. (Ann Arbor, MI) from 1986 to 1997: 10 510(k) clearances. Most are in product codes FPB (Filter, Infusion Line) and GCX (Apparatus, Suction, Operating-Room, Wall…). 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 hospital panel, where it files most

How often FDA has decided Arbor Technologies, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Arbor Technologies, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Arbor Technologies, 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 “Arbor”

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

Arbor Endovascular, LLC 5 Arbor Vita Corportation 1 Arbor Research Corp. 1 Arbor Medical Innovations, LLC 1

Arbor Technologies, Inc.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Arbor”