FDA applicant

Smithkline Beecham Corp.

Parsippany, NJ1 decision1994–19940 recalls

FDA records 1 decision for Smithkline Beecham Corp. (Parsippany, NJ) in 1994: 1 510(k) clearance. All are in product code KOO (Adhesive, Denture, Polyvinyl Methylether…). 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, dental panel, where it files most

How often FDA has decided Smithkline Beecham Corp.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Smithkline Beecham Corp. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Other applicant names beginning “Smithkline”

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

Smithkline Diagnostics, Inc. 42 Smithkline Beecham Consumer Healthcare Products 1

Smithkline Beecham Corp.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Smithkline”