Bovie Medical Corporation Dba Apyx Medical Corporation
United StatesFDA applicant, unverified
- Devices
- 2
What Bovie Medical Corporation Dba Apyx Medical Corporation makes
Bovie Medical Corporation (dba Apyx Medical Corporation) manufactures plasma-based surgical devices, including the Helium Plasma Generator (models APYX-200H/P, APYX-JS3/RS3) and associated Plasma/RF Handpieces. These tools are designed for precise tissue dissection and coagulation in surgical procedures, utilizing plasma technology for controlled cutting and sealing.
The company’s devices are classified as Class II under FDA regulations and are listed in the FDA’s 510(k) registry. The portfolio is regulated in the United States, where Apyx Medical Corporation is based.
Catalogue
- Regimes: 510(k) Registry: 510(k)
Apyx Plasma/RF Handpiece Ref K191542
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Bovie Medical Corporation Dba Apyx Medical Corporation have in the registry?
The registry currently lists 2 devices for Bovie Medical Corporation Dba Apyx Medical Corporation. Devices recorded under merged duplicate company entries are counted once.
Which registries list Bovie Medical Corporation Dba Apyx Medical Corporation's devices?
Among its 2 most recently registered devices, Bovie Medical Corporation Dba Apyx Medical Corporation has devices listed in FDA 510(k) (2 devices).
What risk classes do Bovie Medical Corporation Dba Apyx Medical Corporation's devices fall under?
Among its 2 most recently registered devices, the classes recorded for Bovie Medical Corporation Dba Apyx Medical Corporation's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Bovie Medical Corporation Dba Apyx Medical Corporation in the registry?
The most recently registered devices listed for Bovie Medical Corporation Dba Apyx Medical Corporation include Apyx Helium Plasma Generator (APYX-200H/P, APYX-JS3/RS3) and Apyx Plasma/RF Handpiece.