FDA applicant

Schiff & Co.

West Cadwell, NJ15 decisions1988–19990 recalls

FDA records 15 decisions for Schiff & Co. (West Cadwell, NJ) from 1988 to 1999: 15 510(k) clearances. Most are in product codes LYR (Helicobacter Pylori) and FRA (Purifier, Air, Ultraviolet, Medical). 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, clinical chemistry panel, where it files most

How often FDA has decided Schiff & Co.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Schiff & Co. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Other applicant names beginning “Schiff”

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

Schiff Photo Mechanics 2 Schiff Harding Waite 1

Schiff & Co.

Which product codes does it file in?

Who builds on its devices?

Which of its devices are cited most?

What has FDA decided for it lately?

Other applicant names beginning “Schiff”