Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

Mediott, Inc.

FDA 510(k) & PMA Approved Devices — 2 products

Total Devices2
Categories1
Latest FDA decision2026-03-31
TypeNumberDevice NameCodeDateActions
510(k) K253029 RW-1LLZ2026-03-31 View
510(k) K232456 RW-1LLZ2025-08-11 View
↑