FDA.reportPublic FDA data

ACUITIVE TECHNOLOGIES

FDA Registration(s)#

Registration, FEI, Name table
RegistrationFEINameStatusInitial importerExpiration yearAddress
30145605083014560508ACUITIVE TECHNOLOGIES1N2026-01-0150 Commerce Drive Allendale NJ US 07401

Registered Device Listings#

Registration key, Listing key, Premarket submission table
Registration keyListing keyPremarket submissionDeviceProduct codeDecision date
2832391730537359K240450Citrepore™MQV2024-11-06
2832392053810687K232592CITRELOCK® DUOMBI2023-09-20
2832391447885784K210239CITRESPLINE and CITRELOCK ACL ImplantsMAI2021-02-24
2832391843149031K203334The Citrefix Knotless Suture AnchorMAI2021-02-05
2832391671595692K200725Citregen Tendon Interference Screw and CitrelockMAI2020-10-07

Product Codes Associated With Registrations#

Product code, Registration listing records, Latest decision table
Product codeRegistration listing recordsLatest decision
MAI32021-02-24
MQV12024-11-06
MBI12023-09-20

PMN#