FDA applicant
Safe-Tec Clinical Products, Inc.
FDA records 2 decisions for Safe-Tec Clinical Products, Inc. (Ivyland, PA) from 1988 to 1989: 2 510(k) clearances. Most are in product codes JKA (Tubes, Vials, Systems, Serum Separators, Blood…) and GIO (Tube, Collection, Capillary Blood). 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 Safe-Tec Clinical Products, Inc.’s devices, and how often a recall has named them.
FDA decisions per year
No FDA decision for Safe-Tec Clinical Products, Inc. since 2007.
Recalls per year
No recall linked to its devices since 2007.
Planning a device like Safe-Tec Clinical Products, 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 “Safe-Tec”
FDA records each applicant name separately; these may or may not be the same firm.