Apex T02-110300

GUDID 05391529584641

Apex Tibial Nail Ø 11 x 300mm

ORTHOXEL DESIGNATED ACTIVITY COMPANY

Tibia nail, sterile
Primary Device ID05391529584641
NIH Device Record Key08778d24-5140-4f7a-85cd-8bde1e170144
Commercial Distribution StatusIn Commercial Distribution
Brand NameApex
Version Model NumberT02-110300
Catalog NumberT02-110300
Company DUNS985596830
Company NameORTHOXEL DESIGNATED ACTIVITY COMPANY
Device Count1
DM Exemptfalse
Pre-market Exemptfalse
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usetrue
Lot Batchtrue
Serial Numberfalse
Manufacturing Datefalse
Expiration Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Customer Support Contacts

Phone646-661 3167
Emailcustomercare@orthoxel.com
Phone646-661 3167
Emailcustomercare@orthoxel.com
Phone646-661 3167
Emailcustomercare@orthoxel.com
Phone646-661 3167
Emailcustomercare@orthoxel.com
Phone646-661 3167
Emailcustomercare@orthoxel.com
Phone646-661 3167
Emailcustomercare@orthoxel.com
Phone646-661 3167
Emailcustomercare@orthoxel.com
Phone646-661 3167
Emailcustomercare@orthoxel.com
Phone646-661 3167
Emailcustomercare@orthoxel.com
Phone646-661 3167
Emailcustomercare@orthoxel.com
Phone646-661 3167
Emailcustomercare@orthoxel.com
Phone646-661 3167
Emailcustomercare@orthoxel.com
Phone646-661 3167
Emailcustomercare@orthoxel.com
Phone646-661 3167
Emailcustomercare@orthoxel.com
Phone646-661 3167
Emailcustomercare@orthoxel.com
Phone646-661 3167
Emailcustomercare@orthoxel.com
Phone646-661 3167
Emailcustomercare@orthoxel.com
Phone646-661 3167
Emailcustomercare@orthoxel.com
Phone646-661 3167
Emailcustomercare@orthoxel.com
Phone646-661 3167
Emailcustomercare@orthoxel.com
Phone646-661 3167
Emailcustomercare@orthoxel.com
Phone646-661 3167
Emailcustomercare@orthoxel.com
Phone646-661 3167
Emailcustomercare@orthoxel.com
Phone646-661 3167
Emailcustomercare@orthoxel.com

Device Dimensions

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Operating and Storage Conditions

Special Storage Condition, SpecifyBetween 0 and 0 *Ambient Storage and Handling
Special Storage Condition, SpecifyBetween 0 and 0 *Ambient Storage and Handling
Special Storage Condition, SpecifyBetween 0 and 0 *Ambient Storage and Handling
Special Storage Condition, SpecifyBetween 0 and 0 *Ambient Storage and Handling
Special Storage Condition, SpecifyBetween 0 and 0 *Ambient Storage and Handling
Special Storage Condition, SpecifyBetween 0 and 0 *Ambient Storage and Handling
Special Storage Condition, SpecifyBetween 0 and 0 *Ambient Storage and Handling
Special Storage Condition, SpecifyBetween 0 and 0 *Ambient Storage and Handling
Special Storage Condition, SpecifyBetween 0 and 0 *Ambient Storage and Handling
Special Storage Condition, SpecifyBetween 0 and 0 *Ambient Storage and Handling
Special Storage Condition, SpecifyBetween 0 and 0 *Ambient Storage and Handling
Special Storage Condition, SpecifyBetween 0 and 0 *Ambient Storage and Handling
Special Storage Condition, SpecifyBetween 0 and 0 *Ambient Storage and Handling
Special Storage Condition, SpecifyBetween 0 and 0 *Ambient Storage and Handling
Special Storage Condition, SpecifyBetween 0 and 0 *Ambient Storage and Handling
Special Storage Condition, SpecifyBetween 0 and 0 *Ambient Storage and Handling
Special Storage Condition, SpecifyBetween 0 and 0 *Ambient Storage and Handling
Special Storage Condition, SpecifyBetween 0 and 0 *Ambient Storage and Handling
Special Storage Condition, SpecifyBetween 0 and 0 *Ambient Storage and Handling
Special Storage Condition, SpecifyBetween 0 and 0 *Ambient Storage and Handling
Special Storage Condition, SpecifyBetween 0 and 0 *Ambient Storage and Handling
Special Storage Condition, SpecifyBetween 0 and 0 *Ambient Storage and Handling
Special Storage Condition, SpecifyBetween 0 and 0 *Ambient Storage and Handling
Special Storage Condition, SpecifyBetween 0 and 0 *Ambient Storage and Handling

Device Identifiers

Device Issuing AgencyDevice ID
GS105391529584641 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

HSBRod, Fixation, Intramedullary And Accessories

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2021-02-15
Device Publish Date2021-02-05

On-Brand Devices [Apex]

05391529580797Apex Tibial Endcap
05391529580780Apex Tibia Endcap
05391529580773Apex Tibial Endcap
05391529580582Apex Tibial Nail, Sterile
05391529580193Apex Tibia Screw, Sterile
05391529580186Apex Tibial Screw, Sterile
05391529580179Apex Tibial Screw, Sterile
05391529580162Apex Tibial Screw, Sterile
05391529580155Apex Tibial Screw, Sterile
05391529580148Apex Tibial Screw, Sterile
05391529582180Tibial Extraction Bolt
05391529581459Tibial Insertion Handle
05391529581237Tibial Radiolucent Guide ML
05391529581114Tibial Insertion Bolt
05391529585150Apex Tibial Nailing System Case
05391529584245Yellow Ø4.25mm Drill Sleeve (Length 138.5mm)
05391529584238Trocar Ø8.0mm x Length 150.0mm
05391529584221Green Outer Drill Sleeve (Length 129mm)
05391529584214Suprapatellar AO Mount Anchor Pin
05391529584207AO Mount Drill Extension (Length 136.5mm)
05391529584191Suprapatellar Trocar
05391529584184Suprapatellar K-Wire Guide
05391529584177Suprapatellar Standard Protection Sleeve
05391529584160Suprapatellar Anchoring Protection Sleeve
05391529584153Suprapatellar Protection Sleeve Handle Connector
05391529584146Suprapatellar Protection Sleeve Handle
05391529584139Tibial Suprapatellar Connecting Bolt
05391529584122Tibial Suprapatellar Insert Retainer
05391529584115Tibial Infrapatellar Connecting Bolt
05391529584108Tibial Infrapatellar Insert Retainer
05391529584092Tibial Targeting Guide Locking Bolt
05391529584085Tibial Targeting Guide
05391529584078Tibial Suprapatellar Insertion Handle
05391529584061Tibial Infrapatellar Insertion Handle
05391529584054Ø12 Cannulated Curved Awl
05391529583149Large AO T-Handle
05391529583125Insert Retainer Containing Bolt
05391529583101Monobloc Reamer, Size 8.0
05391529583095Yellow Ø4.25mm Twist Drill X Length 300mm (Use Ø5.00mm Locking Screw)
05391529583088Monobloc Reamer, Size 7.0
05391529583071Locking Screw Length Gauge (Hook)
05391529583064Monobloc Reamer, Size 6.0
05391529583057Flexible IM reamer Shaft 470mm
05391529583040Modular Reamer Head, Size 16.0
05391529583033Modular Reamer Head, Size 15.5
05391529583026Modular Reamer Head, Size 15.0
05391529583019Modular Reamer Head, Size 14.5
05391529583002Modular Reamer Head, Size 14.0
05391529582999Modular Reamer Head, Size 13.5
05391529582982Modular Reamer Head, Size 13.0

Trademark Results [Apex]

Mark Image

Registration | Serial
Company
Trademark
Application Date
APEX
APEX
98811987 not registered Live/Pending
AFTERMARKET PERFORMANCE EXPRESS
2024-10-21
APEX
APEX
98805060 not registered Live/Pending
Dongguan Luxshare Technology Co., Ltd.
2024-10-16
APEX
APEX
98733536 not registered Live/Pending
Apex natural nutrition inc.
2024-09-04
APEX
APEX
98674096 not registered Live/Pending
Medtronic Xomed, Inc.
2024-07-30
APEX
APEX
98673954 not registered Live/Pending
Covert Instruments LLC
2024-07-30
APEX
APEX
98668271 not registered Live/Pending
Smith-Root, Inc.
2024-07-26
APEX
APEX
98662611 not registered Live/Pending
FRC Global Inc.
2024-07-23
APEX
APEX
98644654 not registered Live/Pending
Blume, Phillip James
2024-07-11
APEX
APEX
98636442 not registered Live/Pending
Catalina Carpet Mills Inc.
2024-07-08
APEX
APEX
98616917 not registered Live/Pending
Lander Hospitality Holdings LLC
2024-06-25
APEX
APEX
98616917 not registered Live/Pending
Hines, Victor Nunzio
2024-06-25
APEX
APEX
98616917 not registered Live/Pending
Comes, Bryan
2024-06-25

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