FDA applicant

Beech Medical Products, Inc.

Newtown, PA4 decisions1993–19970 recalls

FDA records 4 decisions for Beech Medical Products, Inc. (Newtown, PA) from 1993 to 1997: 4 510(k) clearances. Most are in product codes FPA (Set, Administration, Intravascular) and FMI (Needle, Hypodermic, Single Lumen). 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 Beech Medical Products, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Beech Medical Products, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Beech Medical Products, 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 “Beech”

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

Beech Medical, Inc. 5

Beech Medical Products, Inc.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Beech”