Ethicon, LLC is one of 19302 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Ethicon, LLC - FDA 510(k) Cleared Devices
Recent clearances: DERMABOND PRINEO Skin Closure System, Coated VICRYU (Polyglactin 91O)Sterile Synthetic Absorbable Suture Cartridges, ETHIBOND Polybutilate Coated Polyester Sterile Synthetic Non-Absorbable Suture Cartridges, PROXISURE Suturing Device
2
Total
2
Cleared
0
Denied
Ethicon, LLC has 2 FDA 510(k) cleared medical devices. Based in Los Frailes Industrial Park, Suite 401, US.
Historical record: 2 cleared submissions from 2016 to 2017. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Ethicon, LLC 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, LLC
2 devices