510(k) Report

FDA applicant

Eastmed Enterprises, Inc.

Marlton, NJ13 decisions1988–19930 recalls

FDA records 13 decisions for Eastmed Enterprises, Inc. (Marlton, NJ) from 1988 to 1993: 13 510(k) clearances. Most are in product codes CCW (Laryngoscope, Rigid) and BWB (Forceps, Tube Introduction). 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, anesthesiology panel, where it files most

How often FDA has decided Eastmed Enterprises, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Eastmed Enterprises, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Eastmed Enterprises, 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 “Eastmed”

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