FDA applicant

Specialty Medical Products Co.

Little Rock, AR4 decisions1987–19930 recalls

FDA records 4 decisions for Specialty Medical Products Co. (Little Rock, AR) from 1987 to 1993: 4 510(k) clearances. Most are in product codes FRG (Wrap, Sterilization) and LRS (I.V. Start Kit). 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 hospital panel, where it files most

How often FDA has decided Specialty Medical Products Co.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Specialty Medical Products Co. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Other applicant names beginning “Specialty”

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

Specialty Surgical Products, Inc. 13 Specialty Ultravision, Inc. 12 Specialty Packaging Producs, Inc. 11 Specialty Appliance Works, Inc. 3 Specialty Medical Industries, Inc. 3 Specialty Water Technologies 2 Specialty Spine Products, LLC 2 Specialty Fibres and Materials, Ltd. 2 Specialty Health Products, Inc. 2 Specialty Dialysis Services 1 Specialty Drives Technologies, Inc. 1 Specialty Tint 1

Specialty Medical Products Co.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Specialty”