FedEx Supply Chain, Inc.

FDA Device Registration & Listing · Memphis, TN, US · Registration 3013403214

Public Record Device Listing Expiry Year: 2026 This page presents structured fields from public FDA datasets.

Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source
FDA Device Registration & Listing
Record Type
Device registration/listing
Registration Number
3013403214
FEI Number
3013403214
Entity Name
FedEx Supply Chain, Inc.
City/State/Country
Memphis, TN, US
Establishment Address
3955 E Holmes Rd, Memphis, TN 38118, US
Establishment Type(s)
Repack or Relabel Medical Device
Owner / Operator
FedEx Supply Chain, Inc. (Owner Number: 10053564)
Owner / Operator Contact Address
3955 East Holmes Rd., Memphis, TN 38118, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
PMA Number
N/A

All Registered Proprietary Names

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Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
KQM Camera, Surgical And Accessories General, Plastic Surgery Class 1 878.4160 2017-09-14
OAD Catheter, Percutaneous, Cardiac Ablation, For Treatment Of Atrial Flutter Unknown Class 3 N/A 2016-12-16
MTD Catheter, Intracardiac Mapping, High-Density Array Cardiovascular Class 2 870.1220 2016-12-16
NFG Device, Communications, Images, Ophthalmic Radiology Class 1 892.2020 2018-06-22
NFF Device, Storage, Images, Ophthalmic Radiology Class 1 892.2010 2018-06-22
HKI Camera, Ophthalmic, Ac-Powered Ophthalmic Class 2 886.1120 2018-06-22
DRF Catheter, Electrode Recording, Or Probe, Electrode Recording Cardiovascular Class 2 870.1220 2016-12-16
HJA Photokeratoscope Ophthalmic Class 1 886.1350 2017-09-14
HMW Drape, Microscope, Ophthalmic General, Plastic Surgery Class 2 878.4370 2017-09-14
HLI Ophthalmoscope, Ac-Powered Ophthalmic Class 2 886.1570 2018-06-28
IYO System, Imaging, Pulsed Echo, Ultrasonic Radiology Class 2 892.1560 2018-06-28
DRF Catheter, Electrode Recording, Or Probe, Electrode Recording Cardiovascular Class 2 870.1220 2016-12-16
FSO Microscope, Surgical, General & Plastic Surgery General, Plastic Surgery Class 1 878.4700 2017-09-14
LMG Agent, Absorbable Hemostatic, Non-Collagen Based General, Plastic Surgery Class 3 878.4490 2018-10-19
OBJ Catheter, Ultrasound, Intravascular Cardiovascular Class 2 870.1200 2016-12-16
FSP Loupe, Diagnostic/Surgical General, Plastic Surgery Class 1 878.4800 2017-09-14
EPT Microscope, Surgical General, Plastic Surgery Class 1 878.4700 2017-09-14
KMN Chair And Table, Medical General Hospital Class 1 880.6140 2017-09-14
EAZ Light, Operating, Dental Dental Class 1 872.4630 2017-09-14
OBJ Catheter, Ultrasound, Intravascular Cardiovascular Class 2 870.1200 2016-12-16
OMD Cutaneous Tissue Adhesive With Mesh General, Plastic Surgery Class 2 878.4011 2018-10-19
OBO Tomography, Optical Coherence Ophthalmic Class 2 886.1570 2018-06-22
HJO Biomicroscope, Slit-Lamp, Ac-Powered Ophthalmic Class 2 886.1850 2018-06-22
LHO Instrument, Quality-Assurance, Radiologic Radiology Class 1 892.1940 2017-09-14
HJO Biomicroscope, Slit-Lamp, Ac-Powered Ophthalmic Class 2 886.1850 2018-06-28
DRF Catheter, Electrode Recording, Or Probe, Electrode Recording Cardiovascular Class 2 870.1220 2018-12-05
GAW Suture, Nonabsorbable, Synthetic, Polypropylene General, Plastic Surgery Class 2 878.5010 2018-10-19
LPB Cardiac Ablation Percutaneous Catheter Unknown Class 3 N/A 2016-12-16
DRF Catheter, Electrode Recording, Or Probe, Electrode Recording Cardiovascular Class 2 870.1220 2016-12-16
GAM Suture, Absorbable, Synthetic, Polyglycolic Acid General, Plastic Surgery Class 2 878.4493 2018-10-19
OBO Tomography, Optical Coherence Ophthalmic Class 2 886.1570 2018-06-22
HKN Refractor, Manual, Non-Powered, Including Phoropter Ophthalmic Class 1 886.1770 2017-09-14
HRM Microscope, Operating & Accessories, Ac-Powered, Ophthalmic General, Plastic Surgery Class 1 878.4700 2017-09-14
OTL Femtosecond Laser System For Refractive Correction Unknown Class 3 N/A 2018-06-22
HKO Refractometer, Ophthalmic Ophthalmic Class 1 886.1760 2017-09-14
HOX Chart, Visual Acuity Ophthalmic Class 1 886.1150 2017-09-14
DRF Catheter, Electrode Recording, Or Probe, Electrode Recording Cardiovascular Class 2 870.1220 2016-12-16
DQK Computer, Diagnostic, Programmable Cardiovascular Class 2 870.1425 2016-12-16
LPB Cardiac Ablation Percutaneous Catheter Unknown Class 3 N/A 2016-12-16
OBJ Catheter, Ultrasound, Intravascular Cardiovascular Class 2 870.1200 2016-12-16
HLI Ophthalmoscope, Ac-Powered Ophthalmic Class 2 886.1570 2018-06-22
MYC Ophthalmoscope, Laser, Scanning Ophthalmic Class 2 886.1570 2018-06-22
HPT Perimeter, Automatic, Ac-Powered Ophthalmic Class 1 886.1605 2017-09-14
LPB Cardiac Ablation Percutaneous Catheter Unknown Class 3 N/A 2016-12-16
OAD Catheter, Percutaneous, Cardiac Ablation, For Treatment Of Atrial Flutter Unknown Class 3 N/A 2016-12-16
OAE Catheter, Percutaneous, Cardiac Ablation, For Treatment Of Atrial Fibrillation Unknown Class 3 N/A 2016-12-16
HMR Marker, Ocular Ophthalmic Class 1 886.4570 2017-09-14
DRF Catheter, Electrode Recording, Or Probe, Electrode Recording Cardiovascular Class 2 870.1220 2018-12-05
DRF Catheter, Electrode Recording, Or Probe, Electrode Recording Cardiovascular Class 2 870.1220 2018-12-05

Official Correspondent

No official correspondent registered.

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

FedEx Supply Chain, Inc.
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

Other Registrations for Same Entity

Registration Number Establishment Name Location
3014197758 FEDEX SUPPLY CHAIN, INC. Olive Branch, MS, US
3015526174 FedEx Supply Chain, Inc. Columbus, OH, US

Related 510(k) Records

510(k) Number Applicant Device Name Decision Date
K241372 ABBOTT MEDICAL Advisor™ HD Grid X Mapping Catheter, Sensor Enabled™ 2024-07-09
K041546 Canon, Inc. DIGITAL FUNDUS CAMERA, MODEL CF-60DSI 2004-06-23
K881966 C.R. Bard, Inc. ELECTROPHYSIOLOGY ELECTRODE CATH. W/SILVER/SILVER 1988-10-04
K192037 ABBOTT MEDICAL Advisor VL Circular Mapping Catheter, Sensor Enabled 2019-09-17
K142953 Optomedical Technologies GmbH OCT-Camera 2015-03-04

Related Recall Records

Recall ID Recalling Firm Recall Class Product Description
Z-0009-2018 Optovue, Inc. 2
iFusion, Device Listing Number D203271. Product Usage: The iCam is a non-contact, high resolution digital imaging device which is suitable for photographing, displaying and storing images of the retina and external areas of the eye to be evaluated under non-mydriatic conditions. The iCam takes digital images of the posterior and external structures of the eye without the use of a mydriatic agent and is intended for use as an aid to clinicians in the evaluation, diagnosis and documentation of ocular health. iCam provides images only and does not provide any diagnostic, pathological analysis or classification of ocular health or disease. AND iVue with Normative Database (K121739) - The iVue is a noncontact, high resolution optical coherence tomography system intended for in vivo imaging, axial cross-sectional, three-dimensional imaging and measurement of anterior and posterior. ocular structures, including retina, retinal nerve fiber layer, ganglion cell complex (GCC), optic disc, cornea, and anterior chamber of the eye. The iVue with Normative Database is a quantitative tool for comparison of retina, retinal nerve fiber layer, ganglion cell complex, and optic disc measurements to a database of known normal subjects.
Z-0008-2018 Optovue, Inc. 2
iVue with Normative Database, Device Listing Number D185549. Product Usage: The iVue (K121739) is a non-contact, high resolution tomographic imaging device. It is intended for in vivo imaging, axial cross-sectional, and three dimensional imaging and measurement of anterior and posterior ocular structures, including retina, retinal nerve fiber layer, ganglion cell complex (GCC), optic disc, cornea, and anterior chamber of the eye. The iVue with Normative Database is a quantitative tool for the comparison of retina, retinal nerve fiber layer, ganglion cell complex, and optic disc measurements to a database of known normal subjects. The iVue with Normative Database is indicated for use as a device to aid in the diagnosis, documentation, and management of ocular health and diseases in the adult population.
Z-0010-2018 Optovue, Inc. 2
iVue 500 with iScan, D216606. Product non-contact, high resolution tomographic imaging device. It is intended for in vivo imaging, axial cross-sectional and three-dimensional imaging and measurement of anterior and posterior ocular structures, including retina, retinal nerve fiber layer, ganglion cell complex (GCC), optic disc, cornea, and anterior chamber of the eye. The iVue 500 with normative database is a quantitative tool for the comparison of retina, retinal nerve fiber layer, ganglion cell complex, and optic disc measurements to a database of known normal subjects. The iVue 500 with normative database is indicated for use as a device to aid in the diagnosis, documentation, and management of ocular health and diseases in the adult population.
Z-0003-2011 Verathon, Inc. 2
BVI 9600 Bladder Volume Instrument, Aorta Scan Mode The BladderScan BVI 9600 with AortaScan Mode is a user-selectable, dual-function ultrasound device that projects ultrasound energy either into the lower abdomen to obtain an image of the bladder for measuring bladder volume, or into the mid-abdomen to obtain an image of the abdominal aorta for aortic diameter measurements.
Z-0004-2011 Verathon, Inc. 2
AortaScan AMI 9700 The AortaScan AMI 9700 is an ultrasound device that projects ultrasound energy into the mid-abdomen to obtain an image of the abdominal aorta for aortic diameter measurements

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3013403214. Last updated year: 2026. Please use registration number 3013403214 when referencing this establishment in official correspondence.
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