FDA applicant
Eastmed Enterprises, Inc.
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
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.
Planning a device like Eastmed Enterprises, Inc.’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 “Eastmed”
FDA records each applicant name separately; these may or may not be the same firm.