FDA applicant
Creative Care Systems, Inc.
FDA records 7 decisions for Creative Care Systems, Inc. (Maplewood, NJ) from 1984 to 1986: 7 510(k) clearances. Most are in product codes FMI (Needle, Hypodermic, Single Lumen) and LJT (Port & Catheter, Implanted, Subcutaneous…). 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 Creative Care Systems, Inc.’s devices, and how often a recall has named them.
FDA decisions per year
No FDA decision for Creative Care Systems, Inc. since 2007.
Recalls per year
No recall linked to its devices since 2007.
Planning a device like Creative Care Systems, 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 “Creative”
FDA records each applicant name separately; these may or may not be the same firm.