FDA applicant

Bruce J. Sand M.D.

Oak Park, CA1 decision2004–20040 recalls

FDA records 1 decision for Bruce J. Sand M.D. (Oak Park, CA) in 2004: 1 510(k) clearance. All are in product code GEX (Powered Laser Surgical Instrument). 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 Bruce J. Sand M.D.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Bruce J. Sand M.D. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Bruce J. Sand M.D. by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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Other applicant names beginning “Bruce”

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

Bruce W. Martin O.D. and Edward Hensley 1 Bruce A. Berkley 1 Bruce Medical Supply 1 Bruce Franklin, Inc. 1 Bruce Mclucas 1

Bruce J. Sand M.D.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Bruce”