Ethicon Endo-Surgery is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Ethicon Endo-Surgery - FDA 510(k) Cleared Devices
Recent clearances: ECHELON LINEAR™ 60 mm Cutter (GLC60), Megadyne Telescoping Smoke Evacuation Pencil - 10ft tubing, Megadyne Telescoping Smoke Evacuation Pencil - 15ft tubing, Megadyne Telescoping Smoke Evacuation Soft Tissue Dissector, Megadyne Telescoping Soft Tissue Dissector
3
Total
2
Cleared
1
Denied
Ethicon Endo-Surgery has 2 FDA 510(k) cleared medical devices. Based in Blue Ash, US.
Last cleared in 2023. Active since 2012. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Ethicon Endo-Surgery Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Ethicon Endo-Surgery, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Ethicon Endo-Surgery
3 devices
Cleared
Mar 15, 2023
ECHELON LINEAR™ 60 mm Cutter (GLC60)
General & Plastic Surgery
90d
Cleared
May 27, 2020
Megadyne Telescoping Smoke Evacuation Pencil - 10ft tubing, Megadyne...
General & Plastic Surgery
114d
Not Cleared
Apr 30, 2012
PERCUTANEOUS SURGICAL SET WITH 5MM OR 10MM ATTACHMENTS
General & Plastic Surgery
222d