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.

Smith & Nephew, Mpl Division

FDA 510(k) & PMA Approved Devices — 9 products

Total Devices9
Categories0
Latest FDA decision
TypeNumberDevice NameCodeDateActions
510(k) K843314 MPL HYPO BRAND BREECH LOAD ASPIR SYRINGEEJI1984-09-27 View
510(k) K841280 SOLOPAK BRAND FILTER NEEDLE W/5 MICROFPB1984-05-21 View
510(k) K840237 MAX-I-PROBE PERIODONTAL ENDODONTIC PROBEIC1984-04-05 View
510(k) K833304 HYPO BRAND DISPOS. DENTAL NEEDLES-PLASTDZM1984-03-30 View
510(k) K832126 MICRO Z DISPOS. SPINAL ANESTH. NEEDLEBSP1983-08-12 View
510(k) K831765 HERAPIN LOCK FLUSH SOLUTION USE KITFMI1983-07-12 View
510(k) K830524 HENKE JECT PRESSURE SYRINGEEJI1983-03-24 View
510(k) K830242 MICRO 2 HYPODERMIC NEEDLESFMI1983-02-15 View
510(k) K761206 INTEROSSEOUS NEEDLEDZM1976-12-13 View
↑