FDA.reportPublic FDA data

IDS

FDA Registration(s)#

Registration, FEI, Name table
RegistrationFEINameStatusInitial importerExpiration yearAddress
30056552873005655287IDS CO, LTD1N2026-01-018-14-30 Nagaminehigashi; Higashi-Ku Kumamoto-Shi JP 861-8038
30071609113007160911IDS KOREA1N2026-01-0110, Gwangnaru-ro 8-gil, Seongdong-Gu 503, Ace Seongsu Tower 1 Seoul KR 04799
30122425943012242594IDS SPA1N2026-01-01VIA VALLETTA SAN CRISTOFORO 28/10 SAVONA IT 17100
30151461063015146106IDS1N2026-01-015425 Exploration Drive Indianapolis IN US 46241

Registered Device Listings#

Registration key, Listing key, Premarket submission table
Registration keyListing keyPremarket submissionDeviceProduct codeDecision date
931601319814645K191902Razor, Everest, U&C LiquidEIH2019-10-11
2373061024162678K162746Ontex and other proprietary namesHEB2017-03-03
931601545263448K143330BruxZir AnteriorEIH2014-12-15
2373061798665924K063641PC-60, NON-INVASIVEPULSE OXIMETERDQA2007-07-13
2373061081665081
2373061177962794
2373061344936108
2373061388667907
931601083668032
1864111112440364
2373061171740174
3499021302661015
2373061507886982
1864111757044743
931601762329006
931602032519945

Product Codes Associated With Registrations#

Product code, Registration listing records, Latest decision table
Product codeRegistration listing recordsLatest decision
EIH22019-10-11
HEB12017-03-03
DQA12007-07-13

PMN#