FDA applicant

Karl M. Block Co.

St. Louis, MO1 decision1985–19851 recall

FDA records 1 decision for Karl M. Block Co. (St. Louis, MO) in 1985: 1 510(k) clearance. All are in product code KNT (Tubes, Gastrointestinal (And Accessories)). 1 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, gastroenterology and urology panel, where it files most

How often FDA has decided Karl M. Block Co.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Karl M. Block Co. since 2007.

Recalls per year

1in 2025

2007high 1 (2025) · low 0 (2007)2026

Class I Class II/III not classified

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

Planning a device like Karl M. Block Co.’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.

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Other applicant names beginning “Karl”

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

KARL STORZ Endoscopy-America, Inc. 370 Karl Storz Endoscopy 35 Karl Storz SE & CO. KG 34 Karl Storz Endoskop GmbH 11 Karl Storz Imaging, Inc. 10 Karl Storz GmbH & Co. (Kst) 1 Karl Storz Lithotripsy-America, Inc. 1 Karl Leibinger GmbH U. Co. KG 1 Karl Storz Endovision, Inc. 1

Karl M. Block Co.

Which product codes does it file in?

What has FDA decided for it lately?

What has been recalled?

Other applicant names beginning “Karl”