Atrix Laboratories, Inc.
United StatesFDA 510(k) applicant, unverified
- Devices
- 3
Catalogue
- 510(k) 510(k)
- 510(k) 510(k)
Atrisorb-D Freeflow Bioabsorbable Guided Tissue Regeneration (Gtr) Barrier With 4% Doxycycline Ref K994137
510(k) 510(k)
Frequently asked questions
How many devices does Atrix Laboratories, Inc. have in the registry?
The registry currently lists 3 devices for Atrix Laboratories, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Atrix Laboratories, Inc.'s devices?
Among its 3 most recently registered devices, Atrix Laboratories, Inc. has devices listed in FDA 510(k) (3 devices).
What risk classes do Atrix Laboratories, Inc.'s devices fall under?
Among its 3 most recently registered devices, the classes recorded for Atrix Laboratories, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Atrix Laboratories, Inc. in the registry?
The most recently registered devices listed for Atrix Laboratories, Inc. include ATRISORB BIOABSORBABLE GUIDED TISSUE REGNERATION(GTR), ATRISORB BIOABSORBABLE GUIDED TISSUE REGENERATION (GTR) BARRIER KIT and ATRISORB-D FREEFLOW BIOABSORBABLE GUIDED TISSUE REGENERATION (GTR) BARRIER WITH 4% DOXYCYCLINE.