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.

G & H Wire Co.

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

Total Devices2
Categories0
Latest FDA decision
TypeNumberDevice NameCodeDateActions
510(k) K081393 ORTHODONTIC TEMPORARY ANCHORAGE IMPLANT SCREWOAT2008-08-21 View
510(k) K961754 SAFETY RELEASE MODULEDZB1996-07-10 View
↑