Ethicon Endo-Sugery, LLC
United StatesFDA 510(k) applicant, unverified
- Devices
- 6
What Ethicon Endo-Sugery, LLC makes
Ethicon Endo-Surgery manufactures laparoscopic surgical accessories, including single-site seal cap assemblies with retractors, biopsy site identifiers for breast and soft tissue procedures, and energy-based cartridge systems for tissue sealing. Their portfolio also includes a tissue sealant designed for laparoscopic and open surgical applications, as well as disposable energy devices for cutting and sealing soft tissue.
These devices are classified as Class II under FDA regulations and are authorised via the 510(k) clearance process. The company is headquartered in the United States.
Catalogue
- 510(k) 510(k)
- 510(k) 510(k)
- 510(k) 510(k)
Ligamax 5 Ref K110699
510(k) 510(k)Ethicon Endo-Surgery Generator G11, Model GEN11 Ref K101990
510(k)Enseal G2 Tissus Sealers Ref K112033
510(k) 510(k)
Frequently asked questions
How many devices does Ethicon Endo-Sugery, LLC have in the registry?
The registry currently lists 6 devices for Ethicon Endo-Sugery, LLC. Devices recorded under merged duplicate company entries are counted once.
Which registries list Ethicon Endo-Sugery, LLC's devices?
Among its 6 most recently registered devices, Ethicon Endo-Sugery, LLC has devices listed in FDA 510(k) (6 devices).
What risk classes do Ethicon Endo-Sugery, LLC's devices fall under?
Among its 6 most recently registered devices, the classes recorded for Ethicon Endo-Sugery, LLC's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Ethicon Endo-Sugery, LLC in the registry?
The most recently registered devices listed for Ethicon Endo-Sugery, LLC include EES SINGLE SITE LAPAROSCOPIC SEAL CAP ASSEMBLY W/ACCESSORIES, MODEL SSL3P, EES FIXED- LENGTH ACCESS RETRACTORS, MAMMOMARK, MAMMOMARK MR AND CORMARK BIOPSY SITE IDENTIFIERS, ECHELON ZEBRA CARTRIDGES, MODELS, Z45WB, Z45BG, Z45GP, Z60WB, Z60BG, ZP60GP and LIGAMAX 5.