FDA.reportPublic FDA data

Kelly Kim

FDA Registration(s)#

Registration, FEI, Name table
RegistrationFEINameStatusInitial importerExpiration yearAddress
30104622743010462274Kelly Kim1N2026-01-0125401 Cabot Rd Ste 122 Laguna Hills CA US 92653

Registered Device Listings#

Registration key, Listing key, Premarket submission table
Registration keyListing keyPremarket submissionDeviceProduct codeDecision date
1879321780004250K251414Miracu™ Polydioxanone (PDO) Suture and Needle (MONO)NEW2025-10-20
1879321772214358K250107V-soft Line™ Barbed Surgical Suture (Various)NEW2025-10-15
1879321076917645K213010FEELject LDV (Low dead volume) syringeQNQ2023-05-31
1879321094480068K172602MiracuNEW2018-11-14
1879321053749852K092831DISPOSABLE HYPODERMIC NEEDLEFMI2010-01-14
1879321487696987
1879321643406924
1879321852069889

Product Codes Associated With Registrations#

Product code, Registration listing records, Latest decision table
Product codeRegistration listing recordsLatest decision
NEW32025-10-20
QNQ12023-05-31
FMI12010-01-14