FDA applicant

Gettig Pharmaceutical Instrument Co.

Spring Mills, PA5 decisions1997–20040 recalls

FDA records 5 decisions for Gettig Pharmaceutical Instrument Co. (Spring Mills, PA) from 1997 to 2004: 5 510(k) clearances. Most are in product codes FMI (Needle, Hypodermic, Single Lumen) and FMF (Syringe, Piston). Its devices cite 8 predicates, 1 of them its own earlier 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 Gettig Pharmaceutical Instrument Co.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Gettig Pharmaceutical Instrument Co. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Gettig Pharmaceutical Instrument Co.

Which product codes does it file in?

Whose devices does it build on?

Which of its devices are cited most?

What has FDA decided for it lately?