FDA applicant

Precision Endoscopy of America, Inc.

Hunt Valley, MD1 decision1997–19970 recalls

FDA records 1 decision for Precision Endoscopy of America, Inc. (Hunt Valley, MD) in 1997: 1 510(k) clearance. All are in product code FDF (Colonoscope And Accessories, Flexible/Rigid). 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 Precision Endoscopy of America, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Precision Endoscopy of America, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Precision Endoscopy of America, Inc.

Which product codes does it file in?

What has FDA decided for it lately?