FDA.reportPublic FDA data

REPROLIFE INC.

FDA Registration(s)#

Registration, FEI, Name table
RegistrationFEINameStatusInitial importerExpiration yearAddress
30130198943013019894REPROLIFE INC.1N2026-01-012-5-3-9F Shinjuku Shinjuku-ku T?ky? JP 160-0022
30180100543018010054Reprolife America, LLC1N2026-01-0122751 Professional Dr Ste 220 Kingwood TX US 77339

Registered Device Listings#

Registration key, Listing key, Premarket submission table
Registration keyListing keyPremarket submissionDeviceProduct codeDecision date
3344501372776948K233846Vitrification Solution Set and Warming Solution SetMQL2024-08-27
2046352067997629K162051CryotecMQK2016-12-14
2046351884381717

Product Codes Associated With Registrations#

Product code, Registration listing records, Latest decision table
Product codeRegistration listing recordsLatest decision
MQL12024-08-27
MQK12016-12-14

PMN#

GUDID#