FDA applicant

Reichert Scientific Instruments

Morris Plains, NJ1 decision1985–19850 recalls

FDA records 1 decision for Reichert Scientific Instruments (Morris Plains, NJ) in 1985: 1 510(k) clearance. All are in product code GCP (Endoscope, Ac-Powered And Accessories). 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, gastroenterology and urology panel, where it files most

How often FDA has decided Reichert Scientific Instruments’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Reichert Scientific Instruments since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Other applicant names beginning “Reichert”

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

Reichert, Inc. 9 Reichert-Jung, Inc. 3 Reichert Ophthalmic Instruments, Div. Leica, Inc. 3

Reichert Scientific Instruments

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Reichert”