Aqua Medical, Inc.
United StatesFDA applicant, unverified
- Devices
- 5
What Aqua Medical, Inc. makes
Aqua Medical, Inc. manufactures radiofrequency (RF) vapor ablation systems designed for tissue removal or coagulation procedures, including those used in dermatology and other medical specialties. These systems employ RF energy to vaporize or ablate targeted tissue, aiding in treatments such as skin resurfacing, lesion removal, or other controlled tissue modifications.
The company’s RF vapor ablation systems are classified as Class II medical devices under US regulations and are listed via the FDA’s 510(k) pathway. These devices are intended for use within the United States, where they are subject to compliance with the FDA’s regulatory requirements for Class II devices.
Catalogue
Aqua Medical RF Vapor System Ref K211282
Regimes: 510(k) Registry: 510(k)Aqua Medical RF Vapor System Ref K183595
Regimes: 510(k) Registry: 510(k)RF Vapor System Ref K213627
Regimes: 510(k) Registry: 510(k)Aqua Medical RF Vapor Ablation System Ref K251226
Regimes: 510(k) Registry: 510(k)Aqua Medical RF Vapor Ablation System Ref K241271
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Aqua Medical, Inc. have in the registry?
The registry currently lists 5 devices for Aqua Medical, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Aqua Medical, Inc.'s devices?
Among its 5 most recently registered devices, Aqua Medical, Inc. has devices listed in FDA 510(k) (5 devices).
What risk classes do Aqua Medical, Inc.'s devices fall under?
Among its 5 most recently registered devices, the classes recorded for Aqua Medical, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Aqua Medical, Inc. in the registry?
The most recently registered devices listed for Aqua Medical, Inc. include Aqua Medical RF Vapor System, RF Vapor System and Aqua Medical RF Vapor Ablation System.