FDA applicant
Bruce W. Martin O.D. and Edward Hensley
FDA records 1 decision for Bruce W. Martin O.D. and Edward Hensley (Gladwin, MI) in 1990: 1 510(k) clearance. All are in product code HPX (Lens, Contact (Polymethylmethacrylate)). 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 Bruce W. Martin O.D. and Edward Hensley’s devices, and how often a recall has named them.
FDA decisions per year
No FDA decision for Bruce W. Martin O.D. and Edward Hensley since 2007.
Recalls per year
No recall linked to its devices since 2007.
Planning a device like Bruce W. Martin O.D. and Edward Hensley’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 “Bruce”
FDA records each applicant name separately; these may or may not be the same firm.