< 회계년도별 의료기기 FDA 등록비용 공지 > Device Registration and Listing Owners or operators of places of business (also called establishments or facilities) that are involved in the production and distribution of medical devices intended for use in the United States (U.S.) are required to register annually with the FDA. This process is known as establishment registration.
Congress has authorized FDA to collect an annual establishment registration fee for device establishment registrations. A detailed list of all those establishment types that have to pay the registration fee can be found at "
Who Must Register, List and Pay the Fee". There are no reductions in annual establishment registration fees for small businesses or any other group
The schedule of registration fees for fiscal years as follows: Year FY 2008 FY 2009 FY 2010 FY 2011 FY 2012
Fee $ 1,706 $ 1,851 $ 2,008 $ 2,179 $ 2,364
Most establishments that are required to register with the FDA are also required to list the devices that are made there and the activities that are performed on those devices. If a device requires premarket approval or notification before being marketed in the U.S., then the owner/operator should also submit the FDA premarket submission number (510(k), PMA, PDP, HDE).
The amendments to the Medical Device User Fee Modernization Act require that after September 30th, 2007, all
registration and listing information be submitted electronically, unless a
waiver has been granted.
Registration and listing provides FDA with the location of medical device establishments and the devices manufactured at those establishments. Knowing where devices are made increases the nation’s ability to prepare for and respond to public health emergencies.
Note: If you encounter an issue or wish to contact us regarding the Electronic Registration and Listing System (FURLS), please send an email to
reglist@cdrh.fda.gov..
