Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

Apollo Endosurgery, Inc.

FDA 510(k) & PMA Approved Devices — 5 products

Total Devices5
Categories3
Latest FDA decision2023-09-18
TypeNumberDevice NameCodeDateActions
510(k) K232544 Apollo ESG NXT System, Apollo REVISE NXT SystemQTD2023-09-18 View
510(k) K231553 OverStitch NXT Endoscopic Suturing SystemOCW2023-06-29 View
510(k) K210266 OverStitch Sx Endoscopic Suturing SystemOCW2021-03-02 View
510(k) K201808 X-Tack Endoscopic HeliX Tacking SystemPKL2020-12-15 View
510(k) K171886 OverStitch SX Endoscopic Suturing System (ESS)OCW2017-11-15 View