Inwound Aps
DenmarkFDA applicant, unverified
- Devices
- 1
What Inwound Aps makes
Inwound Aps manufactures the FlashHeal 2 and FlashHeal 2.0, which are medical devices designed for wound healing and tissue regeneration, likely incorporating advanced wound closure or bio-stimulation technologies.
The company’s portfolio is regulated under Class II devices in the US, with the FlashHeal 2 and FlashHeal 2.0 authorised via the FDA’s 510(k) pathway. The devices are listed in the FDA’s 510(k) registry.
Catalogue
FlashHeal 2 (FlashHeal 2.0) Ref K233077
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Inwound Aps have in the registry?
The registry currently lists 1 device for Inwound Aps. Devices recorded under merged duplicate company entries are counted once.
Which registries list Inwound Aps's devices?
Among its 1 most recently registered device, Inwound Aps has devices listed in FDA 510(k) (1 device).
What risk classes do Inwound Aps's devices fall under?
Among its 1 most recently registered device, the classes recorded for Inwound Aps's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Inwound Aps in the registry?
The most recently registered devices listed for Inwound Aps include FlashHeal 2 (FlashHeal 2.0).