FDA applicant
Retropsoas Technologies, LLC
FDA records 2 decisions for Retropsoas Technologies, LLC (Frontenac, MO) in 2024: 2 510(k) clearances. Most are in product codes ETN (Stimulator, Nerve) and MAX (Intervertebral Fusion Device With Bone Graft…). Its devices cite 3 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 Retropsoas Technologies, LLC’s devices, and how often a recall has named them.
FDA decisions per year
2in 2024
2026 so far, outlined.
Recalls per year
No recall linked to its devices since 2024.
Planning a device like Retropsoas Technologies, LLC’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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