Genesis Medical, Inc.
United StatesFDA applicant, unverified
- Devices
- 2
What Genesis Medical, Inc. makes
Genesis Medical, Inc. manufactures electrosurgical electrode products designed for precise tissue cutting and coagulation in surgical procedures.
These devices are classified as Class II under FDA regulations and are authorised via the 510(k) pathway. The company is based in the United States.
Catalogue
- Regimes: 510(k) Registry: 510(k)
Electrosurgical Electrode Family Ref K992045
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Genesis Medical, Inc. have in the registry?
The registry currently lists 2 devices for Genesis Medical, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Genesis Medical, Inc.'s devices?
Among its 2 most recently registered devices, Genesis Medical, Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do Genesis Medical, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Genesis Medical, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Genesis Medical, Inc. in the registry?
The most recently registered devices listed for Genesis Medical, Inc. include GENESIS TOTAL SHOULDER REPLACEMENT, MODEL 100-01-00 and ELECTROSURGICAL ELECTRODE FAMILY.