Genicon, LC
Country not established
- Devices
- 6
What Genicon, LC makes
Genicon, LC manufactures surgical instruments for minimally invasive procedures, including insufflation needles (120mm), reusable cannulas, shielded trocar/cannula systems, and laparoscopic devices. Their portfolio also includes a clip applier and standalone trocars designed for precision in abdominal and thoracic surgeries.
The company’s products are regulated under FDA’s 510(k) clearance process, with devices classified as Class I and Class II. These instruments are listed in the FDA’s 510(k) registry, and the manufacturer operates from the United States.
Catalogue
Insufflation Needle- 120mm, Model 900-200 Ref K993625
Regimes: 510(k) Registry: 510(k)Reusable Cannula Ref K002542
Regimes: 510(k) Registry: 510(k)Shieldedtrocar/Cannula System, Model 101-005-101 Ref K991382
Regimes: 510(k) Registry: 510(k)Genicon Clip Applier Ref K030269
Regimes: 510(k) Registry: 510(k)Genicon Laparoscopes Ref K030174
Regimes: 510(k) Registry: 510(k)Genicon Trocar Ref K982472
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Genicon, LC have in the registry?
The registry currently lists 6 devices for Genicon, LC. Devices recorded under merged duplicate company entries are counted once.
Which registries list Genicon, LC's devices?
Among its 6 most recently registered devices, Genicon, LC has devices listed in FDA 510(k) (6 devices).
What risk classes do Genicon, LC's devices fall under?
Among its 6 most recently registered devices, the classes recorded for Genicon, LC's devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from Genicon, LC in the registry?
The most recently registered devices listed for Genicon, LC include INSUFFLATION NEEDLE- 120MM, MODEL 900-200, REUSABLE CANNULA, SHIELDEDTROCAR/CANNULA SYSTEM, MODEL 101-005-101 and GENICON CLIP APPLIER.