GLW

FDA Registration(s)#

Registration, FEI, Name table
RegistrationFEINameStatusInitial importerExpiration yearAddress
30149671493014967149GLW, Inc.1Y2026-01-01930 Sylvan Ave Ste 125 Englewood Cliffs NJ US 07632

Registered Device Listings#

Registration key, Listing key, Premarket submission table
Registration keyListing keyPremarket submissionDeviceProduct codeDecision date
2214031421367288K223847CREED™ Cannulated ScrewsHWC2023-01-25
2214031518870198K221489Artemis Proximal Femoral Nail SystemHSB2022-10-27
2214031450043009K213005Apollo Ankle Fracture Plating SystemHRS2022-03-11
2214031707265884K201379Artemis Proximal Femoral Nail SystemHSB2021-02-19
2214031145835105K200343FusionFrame Ring Lock SystemKTT2020-09-14
2214031578825098K200291CREED™ Cannulated ScrewsHWC2020-12-16
2214031599319479K123234ERMIS STERILIZATION CONTAINER SYSTEMKCT2013-07-05
2214031303879171K100857FUSION MEDICAL RING LOCK SYSTEMKTT2010-05-27
2214031005055246
2214031061807666
2214031070463147
2214031072022329
2214031229867797
2214031294440760
2214031357653256
2214031362477744
2214031415183037
2214031528224726
2214031537087393
2214031547029592
2214031859875456
2214031863894214
2214031910375812
2214031965416930
2214031970472543

Product Codes Associated With Registrations#

Product code, Registration listing records, Latest decision table
Product codeRegistration listing recordsLatest decision
HWC22023-01-25
HSB22022-10-27
KTT22020-09-14
HRS12022-03-11
KCT12013-07-05

PMN#

Applications#