FDA applicant

Custom Surgical Products, Inc.

Bossier City, LA4 decisions1984–19880 recalls

FDA records 4 decisions for Custom Surgical Products, Inc. (Bossier City, LA) from 1984 to 1988: 4 510(k) clearances. Most are in product codes GCX (Apparatus, Suction, Operating-Room, Wall…) and GEA (Cannula, Surgical, General & Plastic Surgery). 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 Custom Surgical Products, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

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

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Custom Surgical Products, 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 “Custom”

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

Custom Pack Reliability 21 Custom Spine, Inc. 14 Custom Medical Products, Ltd. 14 Custom Services Intl., Inc. 9 Custom Orthopaedic Solutions, Inc. 8 Custom Ultrasonics 6 Custom Optical Frames, Inc. 4 Custom Medical, Inc. 3 Custom Medical Devices Intl., Inc. 3 Custom Cardio Components 2 Custom Medical Plastics, Inc. 2 Custom Hospitals Products 1

Custom Surgical Products, Inc.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Custom”