Apollo Endosurgery, Inc. - FDA 510(k) Cleared Devices
12
Total
10
Cleared
1
Denied
Apollo Endosurgery, Inc. has 10 FDA 510(k) cleared medical devices. Based in Austin, US.
Last cleared in 2023. Active since 2008. Primary specialty: Gastroenterology & Urology.
Browse the FDA 510(k) cleared devices submitted by Apollo Endosurgery, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) cleared devices by Apollo Endosurgery, Inc.
12 devices
Cleared
Sep 18, 2023
Apollo ESG NXT System, Apollo REVISE NXT System
Gastroenterology & Urology
27d
Cleared
Jun 29, 2023
OverStitch NXT Endoscopic Suturing System
General & Plastic Surgery
30d
Not Cleared
Jul 12, 2022
APOLLO ESG System, APOLLO ESG SX System, APOLLO REVISE System, APOLLO REVISE...
Gastroenterology & Urology
285d
Cleared
Mar 02, 2021
OverStitch Sx Endoscopic Suturing System
General & Plastic Surgery
29d
Cleared
Dec 15, 2020
X-Tack Endoscopic HeliX Tacking System
Gastroenterology & Urology
167d
Cleared
Nov 15, 2017
OverStitch SX Endoscopic Suturing System (ESS)
General & Plastic Surgery
142d
Cleared
Sep 28, 2012
OVERTUBE ENDOSCOPIC ACCESS SYSTEM
Gastroenterology & Urology
60d
Cleared
Oct 28, 2011
SUMO ACCESS AND TISSUE RESECTION SYSTEM
Gastroenterology & Urology
367d
Cleared
Jun 14, 2010
GASTRIC PORT, MODELS: GAP-0016-00, GAP-0018-00, GAP-0020-00
Gastroenterology & Urology
689d
Cleared
Jun 26, 2009
ENDOSCOPIC MONOPOLAR SCISSORS, MODELS EMS-235, EMS-165
Gastroenterology & Urology
114d
Cleared
Dec 19, 2008
ELECTROCAUTERY DILATION BALLOON, MODELS: EDB-0018-00, EDB-0020-00, EDB-0022-00
Gastroenterology & Urology
144d
Cleared
Aug 18, 2008
OVERSTITCH ENDOSCOPIC SUTURE SYSTEM
General & Plastic Surgery
49d