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

Nvision Biomedical Technologies, LLC

FDA 510(k) & PMA Approved Devices — 8 products

Total Devices8
Categories6
Latest Approval2019-04-04
TypeNumberDevice NameCodeDate
510(k) K182943 VERTEX Nitinol Staple System JDR 2019-04-04 View
510(k) K183055 Vector Hammertoe Correction System HWC 2019-02-19 View
510(k) K182949 Healix™ Compression Screw System HWC 2018-12-04 View
510(k) K180458 FOCUS Pedicle Screw System NKB 2018-04-17 View
510(k) K173091 Boundary Anterior Lumbar Buttress Plate KWQ 2017-12-06 View
510(k) K170074 nvc ODP 2017-01-24 View
510(k) K162426 nva, nvp, and nvt MAX 2016-09-29 View
510(k) K161524 Tangis Anterior Cervical Plate KWQ 2016-09-02 View
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