FDA applicant
Excel Health Care Products
FDA records 5 decisions for Excel Health Care Products (S. Plainfield, NJ) from 1985 to 1986: 5 510(k) clearances. Most are in product codes KKX (Drape, Surgical, Antimicrobial) and KDD (Kit, Surgical Instrument, Disposable). 1 recall is linked to its devices.
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) refreshed weekly
How often FDA has decided Excel Health Care Products’s devices, and how often a recall has named them.
FDA decisions per year
No FDA decision for Excel Health Care Products since 2007.
Recalls per year
1in 2019
Class I Class II/III not classified
Planning a device like Excel Health Care Products’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) ReportOther applicant names beginning “Excel”
FDA records each applicant name separately; these may or may not be the same firm.