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.

Inteware Co., Ltd.

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

Total Devices2
Categories2
Latest FDA decision2019-09-12
TypeNumberDevice NameCodeDateActions
510(k) K183695 OrthoAnalysis SoftwarePNN2019-09-12 View
510(k) K173965 Implant Planning SoftwareLLZ2018-10-26 View