FDA applicant

Jack Speer and Assoc., Inc.

Salt Lake City, UT2 decisions2003–20040 recalls

FDA records 2 decisions for Jack Speer and Assoc., Inc. (Salt Lake City, UT) from 2003 to 2004: 2 510(k) clearances. All are in product code JOW (Sleeve, Limb, Compressible). Its devices cite 2 predicates, 0 of them its own earlier devices. 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 Jack Speer and Assoc., Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Jack Speer and Assoc., Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Jack Speer and Assoc., 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 “Jack”

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

Jack W. Kindberg 3 Jack'S Electrodes 2 Jack Martin Co., Inc. 1 Jack H. Ritterskamp 1 Jack Conrey 1 Jack James 1

Jack Speer and Assoc., Inc.

Which product codes does it file in?

Whose devices does it build on?

What has FDA decided for it lately?

Other applicant names beginning “Jack”