Oticon Medical

FDA Filings

This page includes the latest FDA filings for Oticon Medical. Currently, you will find the latest 100 filings for Premarket Notifications, Premarket Applications, De Novo Applications, and GUDID registrations.

FDA Filings

Device Company	Device	Date
PMA P200021S010 Oticon Medical	Neuro Cochlear Implant System	2022-01-14
PMA P200021S009 Oticon Medical	Neuro Cochlear Implant System	2021-11-04
PMA P200021S007 Oticon Medical	Neuro Cochlear Implant System	2021-10-26
PMA P200021S006 Oticon Medical	Neuro Cochlear Implant System	2021-10-26
PMA P200021S005 Oticon Medical	Neuro Cochlear Implant System (“NCIS”)	2021-09-22
PMA P200021S004 Oticon Medical	Neuro Cochlear Implant System	2021-09-10
PMA P200021S003 Oticon Medical	Neuro Cochlear Implant System	2021-09-08
PMA P200021S001 Oticon Medical	Neuro Cochlear Implant System	2021-08-20
PMA P200021 Oticon Medical	Neuro Cochlear Implant System	2021-06-23

Similar & Related FDA Registered Companies

• OTICON MEDICAL, LLC
• Oticon Medical AB
• Oticon Medical2720 Chemin Saint Bernardvallauris 06220 PMA NumberP200021 Supplement NumberS014 Date Received05/18/2022 Decision Date06/17/2022 Product Code MCM  Advisory Committee Ear Nose & Throat Supplement Type30-day Notice Supplement Reason Process Change - Manufacturer/sterilizer/packager/supplier Expedited Review Granted? No
• Oticon Medical2720 Chemin Saint Bernardvallauris 06220 PMA NumberP200021 Supplement NumberS012 Date Received04/29/2022 Decision Date05/27/2022 Product Code MCM  Advisory Committee Ear Nose & Throat Supplement Typenormal 180 Day Track No User Fee Supplement Reason Postapproval Study Protocol Expedited Review Granted? No
• Oticon Medical2720 Chemin Saint Bernardvallauris 06220 PMA NumberP200021 Supplement NumberS011 Date Received02/23/2022 Decision Date03/15/2022 Product Code MCM  Advisory Committee Ear Nose & Throat Supplement Type30-day Notice Supplement Reason Process Change - Manufacturer/sterilizer/packager/supplier Expedited Review Granted? No