FDA applicant

Symbion, Inc.

Salt Lake City, UT2 decisions1987–19880 recalls

FDA records 2 decisions for Symbion, Inc. (Salt Lake City, UT) from 1987 to 1988: 2 510(k) clearances. Most are in product codes LDF (Electrode, Pacemaker, Temporary) and KFM (Pump, Blood, Cardiopulmonary Bypass…). 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 Symbion, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Symbion, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Symbion, 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 “Symbion”

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

Symbion Logistics, LLC 1

Symbion, Inc.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Symbion”