FDA applicant
Wetmore Assoc., Inc.
FDA records 1 decision for Wetmore Assoc., Inc. (Seattle, WA) in 1992: 1 510(k) clearance. All are in product code MIW (Unnamed device). 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 Wetmore Assoc., Inc.’s devices, and how often a recall has named them.
FDA decisions per year
No FDA decision for Wetmore Assoc., Inc. since 2007.
Recalls per year
No recall linked to its devices since 2007.
Planning a device like Wetmore Assoc., Inc.’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