Gibbons Surgical Corp.
United StatesFDA applicant, unverified
- Devices
- 2
What Gibbons Surgical Corp. makes
Gibbons Surgical Corp. manufactures sterile trocar kits designed for laparoscopic and endoscopic surgical procedures. These kits include modified instruments tailored for minimally invasive surgical applications, supporting access and tissue manipulation in abdominal or thoracic cavities.
The company’s products are regulated as Class II medical devices in the US, with individual devices authorised via the FDA’s 510(k) pathway. The portfolio is listed under the FDA’s 510(k) registry, and the manufacturer is based in the United States.
Catalogue
Gibbons Sterile Trocar Kits Ref K012198
Regimes: 510(k) Registry: 510(k)- Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Gibbons Surgical Corp. have in the registry?
The registry currently lists 2 devices for Gibbons Surgical Corp.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Gibbons Surgical Corp.'s devices?
Among its 2 most recently registered devices, Gibbons Surgical Corp. has devices listed in FDA 510(k) (2 devices).
What risk classes do Gibbons Surgical Corp.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Gibbons Surgical Corp.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Gibbons Surgical Corp. in the registry?
The most recently registered devices listed for Gibbons Surgical Corp. include GIBBONS STERILE TROCAR KITS and MODIFICATION TO:LAPAROSCOPIC/ENDOSCOPIC INSTRUMENT.