510(k) Report

FDA applicant

Excel Medical, Inc.

Asbury Park, NJ5 decisions1991–19932 recalls

FDA records 5 decisions for Excel Medical, Inc. (Asbury Park, NJ) from 1991 to 1993: 5 510(k) clearances. Most are in product codes LHI (Set, I.V. Fluid Transfer) and FRN (Pump, Infusion). 2 recalls are 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 Excel Medical, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Excel Medical, Inc. since 2007.

Recalls per year

1in 2014

2014: 1
2007high 1 (2014) · low 0 (2007)2026

Class I Class II/III not classified

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

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

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Other applicant names beginning “Excel”

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