FDA applicant

Dr. Novis Smith & Co., Inc.

Collingswood, NJ1 decision1997–19970 recalls

FDA records 1 decision for Dr. Novis Smith & Co., Inc. (Collingswood, NJ) in 1997: 1 510(k) clearance. All are in product code LRJ (Disinfectant, Medical Devices). 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 Dr. Novis Smith & Co., Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Dr. Novis Smith & Co., Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Dr. Novis Smith & Co., Inc. by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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

See the 510(k) Report

Dr. Novis Smith & Co., Inc.

Which product codes does it file in?

What has FDA decided for it lately?