FDA applicant
Deschutes Medical Products, Inc.
FDA records 8 decisions for Deschutes Medical Products, Inc. (Bend, OR) from 1995 to 2000: 8 510(k) clearances. Most are in product codes HHW (Pessary, Vaginal) and HIR (Perineometer). Its devices cite 1 predicate, 1 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 Deschutes Medical Products, Inc.’s devices, and how often a recall has named them.
FDA decisions per year
No FDA decision for Deschutes Medical Products, Inc. since 2007.
Recalls per year
No recall linked to its devices since 2007.
Planning a device like Deschutes Medical Products, Inc.’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.
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