FDA applicant
Soflex Contact Lens Industries, Ltd.
FDA records 6 decisions for Soflex Contact Lens Industries, Ltd. (Littleton, CO) from 2001 to 2004: 6 510(k) clearances. All are in product code LPL (Lenses, Soft Contact, Daily Wear). 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 Soflex Contact Lens Industries, Ltd.’s devices, and how often a recall has named them.
FDA decisions per year
No FDA decision for Soflex Contact Lens Industries, Ltd. since 2007.
Recalls per year
No recall linked to its devices since 2007.
Planning a device like Soflex Contact Lens Industries, Ltd.’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 “Soflex”
FDA records each applicant name separately; these may or may not be the same firm.