ASY-01078

GUDID 00840200409261

Tab Grabber Assembly

Integrity Implants Inc.

General internal orthopaedic fixation system implantation kit
Primary Device ID00840200409261
NIH Device Record Key4de417ab-1b8c-497c-8553-5afd26429ba0
Commercial Distribution StatusIn Commercial Distribution
Version Model NumberASY-01078
Catalog NumberASY-01078
Company DUNS080300717
Company NameIntegrity Implants Inc.
Device Count1
DM Exemptfalse
Pre-market Exempttrue
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usefalse
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

Phone8002019300
Emailcustomerservice@integrityimplants.com
Phone8002019300
Emailcustomerservice@integrityimplants.com
Phone8002019300
Emailcustomerservice@integrityimplants.com
Phone8002019300
Emailcustomerservice@integrityimplants.com
Phone8002019300
Emailcustomerservice@integrityimplants.com
Phone8002019300
Emailcustomerservice@integrityimplants.com
Phone8002019300
Emailcustomerservice@integrityimplants.com
Phone8002019300
Emailcustomerservice@integrityimplants.com
Phone8002019300
Emailcustomerservice@integrityimplants.com
Phone8002019300
Emailcustomerservice@integrityimplants.com
Phone8002019300
Emailcustomerservice@integrityimplants.com
Phone8002019300
Emailcustomerservice@integrityimplants.com
Phone8002019300
Emailcustomerservice@integrityimplants.com
Phone8002019300
Emailcustomerservice@integrityimplants.com
Phone8002019300
Emailcustomerservice@integrityimplants.com
Phone8002019300
Emailcustomerservice@integrityimplants.com
Phone8002019300
Emailcustomerservice@integrityimplants.com

Device Identifiers

Device Issuing AgencyDevice ID
GS100840200409261 [Primary]

FDA Product Code

LXHOrthopedic Manual Surgical Instrument

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[00840200409261]

Moist Heat or Steam Sterilization


[00840200409261]

Moist Heat or Steam Sterilization


[00840200409261]

Moist Heat or Steam Sterilization


[00840200409261]

Moist Heat or Steam Sterilization


[00840200409261]

Moist Heat or Steam Sterilization


[00840200409261]

Moist Heat or Steam Sterilization


[00840200409261]

Moist Heat or Steam Sterilization


[00840200409261]

Moist Heat or Steam Sterilization


[00840200409261]

Moist Heat or Steam Sterilization


[00840200409261]

Moist Heat or Steam Sterilization


[00840200409261]

Moist Heat or Steam Sterilization


[00840200409261]

Moist Heat or Steam Sterilization


[00840200409261]

Moist Heat or Steam Sterilization


[00840200409261]

Moist Heat or Steam Sterilization


[00840200409261]

Moist Heat or Steam Sterilization


[00840200409261]

Moist Heat or Steam Sterilization


[00840200409261]

Moist Heat or Steam Sterilization


Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2023-10-03
Device Publish Date2023-09-25

Devices Manufactured by Integrity Implants Inc.

00840200410229 - NA2024-10-28 5.5-6.0 MIS Counter Torque - No Lip
00840200402477 - LineSider2024-10-25 5.5/6.0mm, Non-mod Standard 7.1mm- Iliac Shank - 9.5mm x 90mm
00840200407373 - N/A2024-10-25 Open Disc Prep Insert 2
00840200405492 - NA2024-09-09 BH Tapered Screw Starter
00840200410045 - N/A2024-07-18 SS Right Blade, 80mm
00840200410052 - N/A2024-07-18 SS Right Blade, 70mm
00840200410069 - N/A2024-07-18 SS Right Blade, 60mm
00840200410076 - N/A2024-07-18 SS Right Blade, 50mm

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