FDA applicant
Symtex Healthcare Corp.
FDA records 1 decision for Symtex Healthcare Corp. (Walnut, CA) in 1999: 1 510(k) clearance. All are in product code EFQ (Gauze/Sponge, Internal). 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 Symtex Healthcare Corp.’s devices, and how often a recall has named them.
FDA decisions per year
No FDA decision for Symtex Healthcare Corp. since 2007.
Recalls per year
No recall linked to its devices since 2007.
Planning a device like Symtex Healthcare Corp.’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) Report