FDA applicant

Arbor Research Corp.

Ann Arbor, MI1 decision1997–19970 recalls

FDA records 1 decision for Arbor Research Corp. (Ann Arbor, MI) in 1997: 1 510(k) clearance. All are in product code CAW (Generator, Oxygen, Portable). 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, anesthesiology panel, where it files most

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

FDA decisions per year

No FDA decision for Arbor Research Corp. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Arbor Research Corp. 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 Technologies, Inc. 10 Arbor Endovascular, LLC 5 Arbor Vita Corportation 1 Arbor Medical Innovations, LLC 1

Arbor Research Corp.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Arbor”