Puregraft, LLC
United StatesFDA 510(k) applicant, unverified
- Devices
- 14
What Puregraft, LLC makes
Puregraft, LLC manufactures Dermapose Access and Dermapose Refresh, which are medical devices designed for wound care and tissue preparation. These products are intended for use in surgical and dermatological procedures, including debridement and skin grafting applications.
The company’s portfolio is regulated under FDA Class II devices and requires 510(k) clearance for market authorisation. The devices are listed in the FDA’s 510(k) database. Puregraft, LLC is based in the United States.
Catalogue
Search and filter all 14 devicesCompany details
- DUNS number
- 079508934
- [email protected]
- Phone
- 858-348-8050
Frequently asked questions
How many devices does Puregraft, LLC have in the registry?
The registry currently lists 14 devices for Puregraft, LLC. Devices recorded under merged duplicate company entries are counted once.
Which registries list Puregraft, LLC's devices?
Among its 14 most recently registered devices, Puregraft, LLC has devices listed in FDA 510(k) (2 devices) and FDA GUDID (12 devices). A device can be listed in more than one registry, so these counts overlap.
What risk classes do Puregraft, LLC's devices fall under?
Among its 14 most recently registered devices, the classes recorded for Puregraft, LLC's devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from Puregraft, LLC in the registry?
The most recently registered devices listed for Puregraft, LLC include Puregraft MicroFat Transfer Kit (19G) 50/MICRO19, Puregraft 850, Dermapose Refresh Syringe Stand and AutoPose Restore ABS-101035-1.