Surgicon, Inc.
United StatesFDA applicant, unverified
- Devices
- 2
What Surgicon, Inc. makes
Surgicon, Inc. manufactures laparoscopic gallbladder extraction devices, including the DEGALL II and DEGALL laparoscopic gallbladder extractors. These tools are designed for minimally invasive surgical procedures to remove the gallbladder through small incisions, aiding in the recovery and management of biliary conditions.
The company’s portfolio is classified under FDA’s Class II regulatory category and is listed via the 510(k) clearance process. These devices are intended for use in the United States, adhering to the country’s medical device regulations.
Catalogue
Degall Ii Gallbladder Extractor Ref K033359
Regimes: 510(k) Registry: 510(k)Degall Laparoscopic Gallbladder Extractor Ref K021747
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Surgicon, Inc. have in the registry?
The registry currently lists 2 devices for Surgicon, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Surgicon, Inc.'s devices?
Among its 2 most recently registered devices, Surgicon, Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do Surgicon, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Surgicon, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Surgicon, Inc. in the registry?
The most recently registered devices listed for Surgicon, Inc. include DEGALL II GALLBLADDER EXTRACTOR and DEGALL LAPAROSCOPIC GALLBLADDER EXTRACTOR.