OverStitch Endoscopic Suturing System Sx ESS-G02-Sx1

GUDID 20811955020715

Needle Driver and Anchor Exchange

Apollo Endosurgery, Inc.

Suturing unit, single-use Suturing unit, single-use Suturing unit, single-use Suturing unit, single-use Suturing unit, single-use Suturing unit, single-use Suturing unit, single-use Suturing unit, single-use Suturing unit, single-use Suturing unit, single-use Suturing unit, single-use Suturing unit, single-use Suturing unit, single-use Suturing unit, single-use Suturing unit, single-use Suturing unit, single-use Suturing unit, single-use Suturing unit, single-use Suturing unit, single-use Suturing unit, single-use Suturing unit, single-use Suturing unit, single-use Suturing unit, single-use Suturing unit, single-use Suturing unit, single-use Suturing unit, single-use Suturing unit, single-use Suturing unit, single-use Suturing unit, single-use Suturing unit, single-use Suturing unit, single-use Suturing unit, single-use Suturing unit, single-use
Primary Device ID20811955020715
NIH Device Record Keyf4df2b05-0d3a-4361-8bfe-844b51dced97
Commercial Distribution StatusIn Commercial Distribution
Brand NameOverStitch Endoscopic Suturing System Sx
Version Model NumberESS-G02-Sx1
Catalog NumberESS-G02-Sx1
Company DUNS625064352
Company NameApollo Endosurgery, Inc.
Device Count1
DM Exemptfalse
Pre-market Exemptfalse
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kittrue
Device Combination Productfalse
Single Usetrue
Lot Batchtrue
Serial Numbertrue
Manufacturing Datefalse
Expiration Datetrue
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Customer Support Contacts

Phone855-551-3123
Emailproductcomplaints.us@apolloendo.com
Phone855-551-3123
Emailproductcomplaints.us@apolloendo.com
Phone855-551-3123
Emailproductcomplaints.us@apolloendo.com
Phone855-551-3123
Emailproductcomplaints.us@apolloendo.com
Phone855-551-3123
Emailproductcomplaints.us@apolloendo.com
Phone855-551-3123
Emailproductcomplaints.us@apolloendo.com
Phone855-551-3123
Emailproductcomplaints.us@apolloendo.com
Phone855-551-3123
Emailproductcomplaints.us@apolloendo.com
Phone855-551-3123
Emailproductcomplaints.us@apolloendo.com
Phone855-551-3123
Emailproductcomplaints.us@apolloendo.com
Phone855-551-3123
Emailproductcomplaints.us@apolloendo.com
Phone855-551-3123
Emailproductcomplaints.us@apolloendo.com
Phone855-551-3123
Emailproductcomplaints.us@apolloendo.com
Phone855-551-3123
Emailproductcomplaints.us@apolloendo.com
Phone855-551-3123
Emailproductcomplaints.us@apolloendo.com
Phone855-551-3123
Emailproductcomplaints.us@apolloendo.com
Phone855-551-3123
Emailproductcomplaints.us@apolloendo.com
Phone855-551-3123
Emailproductcomplaints.us@apolloendo.com
Phone855-551-3123
Emailproductcomplaints.us@apolloendo.com
Phone855-551-3123
Emailproductcomplaints.us@apolloendo.com
Phone855-551-3123
Emailproductcomplaints.us@apolloendo.com
Phone855-551-3123
Emailproductcomplaints.us@apolloendo.com
Phone855-551-3123
Emailproductcomplaints.us@apolloendo.com
Phone855-551-3123
Emailproductcomplaints.us@apolloendo.com
Phone855-551-3123
Emailproductcomplaints.us@apolloendo.com
Phone855-551-3123
Emailproductcomplaints.us@apolloendo.com
Phone855-551-3123
Emailproductcomplaints.us@apolloendo.com
Phone855-551-3123
Emailproductcomplaints.us@apolloendo.com
Phone855-551-3123
Emailproductcomplaints.us@apolloendo.com
Phone855-551-3123
Emailproductcomplaints.us@apolloendo.com
Phone855-551-3123
Emailproductcomplaints.us@apolloendo.com
Phone855-551-3123
Emailproductcomplaints.us@apolloendo.com
Phone855-551-3123
Emailproductcomplaints.us@apolloendo.com

Device Identifiers

Device Issuing AgencyDevice ID
GS110811955020718 [Primary]
GS120811955020715 [Package]
Contains: 10811955020718
Package: Case [3 Units]
In Commercial Distribution

FDA Product Code

HCFInstrument, Ligature Passing And Knot Tying

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2021-06-03
Device Publish Date2021-05-26

Devices Manufactured by Apollo Endosurgery, Inc.

00811955020896 - OverStitch NXT Endoscopic Suturing System2023-11-24 Needle Driver and Anchor Exchange
10811955020916 - NXT Tissue Helix Pro2023-11-24 Tissue Helix
00811955020933 - Apollo ESG NXT System2023-11-24 Single Channel Endobariatric System
00811955020940 - Apollo Revise NXT System2023-11-24 Single Channel Endobariatric System
00811955020780 - APOLLO ESG™ System2023-05-15 Dual Channel Endobariatric System
00811955020797 - APOLLO ESG Sx™ System2023-05-15 Single Channel Endobariatric System
00811955020803 - APOLLO Revise™ System2023-05-15 Dual Channel Endobariatric System
00811955020810 - APOLLO REVISE™ Sx System2023-05-15 Single Channel Endobariatric System

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