Ad-Tech Medical Instrument Corporation is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Ad-Tech Medical Instrument Corporation - FDA 510(k) Cleared Devices
Recent clearances: Spencer Probe Depth Electrodes, Anchor Bolts as Accessories to Depth Electrodes, Subdural Strip/Intraoperative Split Electrode, Subdural Grid/Intraoperative Grid Electrode, Dual-Sided Interhemispheric Subdural Electrode, Multi-Strip and Slit Grid Subdural Electrode, Intraoperative Mapping Grid Subdural Electrode
8
Total
8
Cleared
0
Denied
Ad-Tech Medical Instrument Corporation has 8 FDA 510(k) cleared medical devices. Based in Racine, US.
Last cleared in 2023. Active since 2016. Primary specialty: Neurology.
Browse the FDA 510(k) cleared devices submitted by Ad-Tech Medical Instrument Corporation Filter by specialty or product code using the sidebar.
Regulatory submissions have been managed by Quality & Regulatory Associates, LLC and Namsa Medical Research Organization.
FDA 510(k) Regulatory Record - Ad-Tech Medical Instrument Corporation
8 devices
Cleared
May 18, 2023
Spencer Probe Depth Electrodes
Neurology
206d
Cleared
May 18, 2023
Anchor Bolts as Accessories to Depth Electrodes
Neurology
206d
Cleared
Jan 25, 2020
Subdural Strip/Intraoperative Split Electrode, Subdural Grid/Intraoperative...
Neurology
267d
Cleared
Aug 09, 2018
Anchor Bolt (as an accessory to Depth Electrodes)
Neurology
58d
Cleared
Sep 07, 2017
Cranial Drill Bits and Accessories
Neurology
205d
Cleared
Apr 12, 2017
Depth Electrodes, Foramen Ovale Depth Eletrodes, Marco-Micro Depth...
Neurology
133d
Cleared
May 06, 2016
FREMAP ELECTRODE
Ear, Nose, Throat
224d
Cleared
Mar 04, 2016
DNAP Electrode
Neurology
178d