Cintron Medical Corporation
United Statesfrom the FDA registration address FDA establishment FEI 3006266622
- Devices
- 2
- Registrations
- FDA
- FDA recalls
- 0
What Cintron Medical Corporation makes
CINTRON Medical Corporation manufactures the gi2000 Electrosurgical Generator, a device designed for controlled tissue cutting and coagulation in surgical procedures. This generator provides precise energy delivery for procedures in various medical specialties, including general surgery and gynecology.
The company’s portfolio is regulated under Class II devices in the United States, with the gi2000 Electrosurgical Generator listed via the FDA’s 510(k) pathway. CINTRON Medical Corporation is headquartered in the US.
Catalogue
- Registry: GUDID
gi2000 Electrosurgical Generator Ref K250657
Regimes: 510(k) Registry: 510(k)
Company details
- FDA FEI number
- 3006266622
- Address
- 1275 W 124th Ave, WESTMINSTER, CO, 80234
Frequently asked questions
How many devices does CINTRON MEDICAL CORPORATION have in the registry?
The registry currently lists 2 devices for CINTRON MEDICAL CORPORATION. Devices recorded under merged duplicate company entries are counted once.
Which registries list CINTRON MEDICAL CORPORATION's devices?
Among its 2 most recently registered devices, CINTRON MEDICAL CORPORATION has devices listed in FDA 510(k) (1 device) and FDA GUDID (1 device). A device can be listed in more than one registry, so these counts overlap.
What risk classes do CINTRON MEDICAL CORPORATION's devices fall under?
Among its 2 most recently registered devices, the classes recorded for CINTRON MEDICAL CORPORATION's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from CINTRON MEDICAL CORPORATION in the registry?
The most recently registered devices listed for CINTRON MEDICAL CORPORATION include GI2000 30-0026-xxx and gi2000 Electrosurgical Generator.