FDA applicant
No 7 Contact Lens Laboratory, Ltd.
FDA records 1 decision for No 7 Contact Lens Laboratory, Ltd. (Grand Junction, CO) in 2003: 1 510(k) clearance. All are in product code LPL (Lenses, Soft Contact, Daily Wear). Its devices cite 4 predicates, 0 of them its own earlier devices. 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 No 7 Contact Lens Laboratory, Ltd.’s devices, and how often a recall has named them.
FDA decisions per year
No FDA decision for No 7 Contact Lens Laboratory, Ltd. since 2007.
Recalls per year
No recall linked to its devices since 2007.
Planning a device like No 7 Contact Lens Laboratory, 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) Report