Aesthera Corporation
United StatesFDA applicant, unverified
- Devices
- 3
What Aesthera Corporation makes
Aesthera Corporation manufactures the Photopneumatic (PPX) System for non-invasive skin treatment, the Intensive Pulsed Light (IPL) System for hair removal and vascular lesion therapy, and the ISOLAZ device for acne treatment using blue light therapy.
These devices are classified as Class II under FDA regulations and are listed via the 510(k) clearance process. The company is based in the United States.
Catalogue
Aesthera Photopneumatic (Ppx) System Ref K062048
Regimes: 510(k) Registry: 510(k)Aip Intense Pulsed Light System Ref K041554
Regimes: 510(k) Registry: 510(k)Isolaz Ref K083730
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Aesthera Corporation have in the registry?
The registry currently lists 3 devices for Aesthera Corporation. Devices recorded under merged duplicate company entries are counted once.
Which registries list Aesthera Corporation's devices?
Among its 3 most recently registered devices, Aesthera Corporation has devices listed in FDA 510(k) (3 devices).
What risk classes do Aesthera Corporation's devices fall under?
Among its 3 most recently registered devices, the classes recorded for Aesthera Corporation's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Aesthera Corporation in the registry?
The most recently registered devices listed for Aesthera Corporation include AESTHERA PHOTOPNEUMATIC (PPX) SYSTEM, AIP INTENSE PULSED LIGHT SYSTEM and ISOLAZ.