FDA applicant

Effner and Spreine Co.

Port Washington, NY4 decisions1985–19880 recalls

FDA records 4 decisions for Effner and Spreine Co. (Port Washington, NY) from 1985 to 1988: 4 510(k) clearances. Most are in product codes CCW (Laryngoscope, Rigid) and KNT (Tubes, Gastrointestinal (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 Effner and Spreine Co.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Effner and Spreine Co. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Effner and Spreine Co.’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.

See the 510(k) Report

Other applicant names beginning “Effner”

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

Effner, Inc. 3

Effner and Spreine Co.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Effner”