LAP-BAND System Adjustment Kit B-20310

GUDID 10811955020015

PRI PACK LAP-BAND ADJUSTMENT KIT (APOLLO)

Apollo Endosurgery, Inc.

Subcutaneous infusion/injection port needle Subcutaneous infusion/injection port needle Subcutaneous infusion/injection port needle Subcutaneous infusion/injection port needle Subcutaneous infusion/injection port needle Subcutaneous infusion/injection port needle Subcutaneous infusion/injection port needle Subcutaneous infusion/injection port needle Subcutaneous infusion/injection port needle Subcutaneous infusion/injection port needle Subcutaneous infusion/injection port needle Subcutaneous infusion/injection port needle Subcutaneous infusion/injection port needle Subcutaneous infusion/injection port needle

• Primary Device ID: 10811955020015
• NIH Device Record Key: 11a30c89-69c5-4ba1-a31c-75a991a22f02
• Commercial Distribution Discontinuation: 2020-11-20
• Commercial Distribution Status: Not in Commercial Distribution
• Brand Name: LAP-BAND System Adjustment Kit
• Version Model Number: B-20310
• Catalog Number: B-20310
• Company DUNS: 625064352
• Company Name: Apollo Endosurgery, Inc.
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: false
• MRI Safety Status: Labeling does not contain MRI Safety Information
• Human Cell/Tissue Product: false
• Device Kit: false
• Device Combination Product: false
• Single Use: true
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: false
• Expiration Date: true
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: true
• OTC Over-The-Counter: false

Customer Support Contacts

• Phone: 855-551-3123
• Email: productcomplaints.us@apolloendo.com
• Phone: 855-551-3123
• Email: productcomplaints.us@apolloendo.com
• Phone: 855-551-3123
• Email: productcomplaints.us@apolloendo.com
• Phone: 855-551-3123
• Email: productcomplaints.us@apolloendo.com
• Phone: 855-551-3123
• Email: productcomplaints.us@apolloendo.com
• Phone: 855-551-3123
• Email: productcomplaints.us@apolloendo.com
• Phone: 855-551-3123
• Email: productcomplaints.us@apolloendo.com
• Phone: 855-551-3123
• Email: productcomplaints.us@apolloendo.com
• Phone: 855-551-3123
• Email: productcomplaints.us@apolloendo.com
• Phone: 855-551-3123
• Email: productcomplaints.us@apolloendo.com
• Phone: 855-551-3123
• Email: productcomplaints.us@apolloendo.com
• Phone: 855-551-3123
• Email: productcomplaints.us@apolloendo.com
• Phone: 855-551-3123
• Email: productcomplaints.us@apolloendo.com
• Phone: 855-551-3123
• Email: productcomplaints.us@apolloendo.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	10811955020015 [Primary]
GS1	30811955020019 [Package]; Package: Kit [10 Units]; Discontinued: 2020-11-20; Not in Commercial Distribution

FDA Product Code

• LTI: Implant, Intragastric For Morbid Obesity

Sterilization

• Steralize Prior To Use: false
• Device Is Sterile: true

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 4
• Public Version Date: 2021-01-08
• Device Publish Date: 2014-09-15

Devices Manufactured by Apollo Endosurgery, Inc.

• 00811955020896 - OverStitch NXT Endoscopic Suturing System: 2023-11-24 Needle Driver and Anchor Exchange
• 10811955020916 - NXT Tissue Helix Pro: 2023-11-24 Tissue Helix
• 00811955020933 - Apollo ESG NXT System: 2023-11-24 Single Channel Endobariatric System
• 00811955020940 - Apollo Revise NXT System: 2023-11-24 Single Channel Endobariatric System
• 00811955020780 - APOLLO ESG™ System: 2023-05-15 Dual Channel Endobariatric System
• 00811955020797 - APOLLO ESG Sx™ System: 2023-05-15 Single Channel Endobariatric System
• 00811955020803 - APOLLO Revise™ System: 2023-05-15 Dual Channel Endobariatric System
• 00811955020810 - APOLLO REVISE™ Sx System: 2023-05-15 Single Channel Endobariatric System