FDA applicant

Arch Development Group

St. Louis, MO2 decisions1991–19910 recalls

FDA records 2 decisions for Arch Development Group (St. Louis, MO) in 1991: 2 510(k) clearances. Most are in product codes KKX (Drape, Surgical, Antimicrobial) and MHW (Dressing, Compression). 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 Arch Development Group’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Arch Development Group since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Arch Development Group by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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Other applicant names beginning “Arch”

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

Arch Therapeutics, Inc. 2 Arch Catheter, LLC 1

Arch Development Group

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Arch”