FDA applicant
Metricon, Ltd.
FDA records 3 decisions for Metricon, Ltd. (Walker, MI) from 1980 to 1981: 3 510(k) clearances. Most are in product codes EWG (Laser, Ent Microsurgical Carbon-Dioxide) and HHR (Laser, Surgical, Gynecologic). 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 Metricon, Ltd.’s devices, and how often a recall has named them.
FDA decisions per year
No FDA decision for Metricon, Ltd. since 2007.
Recalls per year
No recall linked to its devices since 2007.
Planning a device like Metricon, 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