FDA applicant

Aspen Surgical Products, Inc.

Byron Center, MI2 decisions2002–20030 recalls

FDA records 2 decisions for Aspen Surgical Products, Inc. (Byron Center, MI) from 2002 to 2003: 2 510(k) clearances. Most are in product codes GEI (Electrosurgical, Cutting & Coagulation &…) and FTA (Light, Surgical, 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 Aspen Surgical Products, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Aspen Surgical Products, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Aspen Surgical Products, Inc. by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

Planning a device like Aspen Surgical Products, Inc.’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.

See the 510(k) Report

Other applicant names beginning “Aspen”

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

Aspen Laboratories, Inc. 55 Aspen Labs 6 Aspen Glove Sdn. Bhd. 4 Aspen Laser Systems, LLC 2 Aspen Imaging Healthcare, Inc. 2 Aspen Medical, Ltd. 1

Aspen Surgical Products, 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?

Other applicant names beginning “Aspen”