FDA applicant

Esco Precision, Inc.

Stony Brook, NY3 decisions1990–19910 recalls

FDA records 3 decisions for Esco Precision, Inc. (Stony Brook, NY) from 1990 to 1991: 3 510(k) clearances. Most are in product codes FCL (Forceps, Biopsy, Non-Electric) and KGE (Forceps, Biopsy, Electric). 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 Esco Precision, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Esco Precision, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Other applicant names beginning “Esco”

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

Esco Medical 1

Esco Precision, Inc.

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 “Esco”